Multiplex homology-directed repair

ABSTRACT

Disclosed is a method for introducing a plurality of programmed nucleotide modifications into a single locus of a desired genomic DNA sequence in a single experiment. The method entails synthesizing a homology-directed repair (HDR) library comprising a plurality of oligonucleotides, wherein each oligonucleotide comprises a programmed nucleotide modification in the locus of the desired genome, and co-transfecting a population of cells with (i) an expression system capable of expressing Cas9 and a single guide RNA (sgRNA) and (ii) introducing a plurality of programmed nucleotide modifications to the locus of the desired genomic DNA sequence in one or more cells of the population. Also disclosed are methods for analyzing the functional consequence of a genomic mutation and for genomic screening.

PRIORITY CLAIM

This application claims priority to U.S. Provisional Patent ApplicationNo. 62/032,734, filed Aug. 4, 2014, and U.S. Provisional PatentApplication No. 62/046,074, filed Sep. 4, 2014, the subject matters ofwhich are hereby incorporated by reference in their entireties as iffully set forth herein.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

This invention was made with government support under Grant No.DP1HG007811, awarded by the National Institutes of Health. Thegovernment has certain rights in the invention.

BACKGROUND

Saturation mutagenesis [1, 2]—coupled to an appropriate biologicalassay—represents a fundamental means of achieving a high-resolutionunderstanding of regulatory [3] and protein-coding [4] nucleic acidsequences of interest. However, mutagenized sequences introduced intrans on episomes or via random or “safe-harbour” integration fail tocapture the native context of the endogenous chromosomal locus [5]. Thisshortcoming markedly limits the interpretability of the resultingmeasurements of mutational impact.

Functional consequences of genetic variants are studied by manipulatingthe endogenous locus, which provides the native chromosomal context withrespect to DNA sequence and epigenetic milieu, and for proteins,endogenous levels and patterns of expression [6]. Programmableendonucleases, e.g. zinc-finger nucleases (ZFNs), transcriptionactivator-like effector nucleases (TALENs) or clustered regularlyinterspaced short palindromic repeat (CRISPR)/Cas-based RNA-guided DNAendonucleases, enable direct genome editing with increasing practicality[7]. However, genome editing has primarily been applied to introducesingle changes to one or a few genomic loci [8], rather than manyprogrammed changes to a single genomic locus. There remains a need for agenomic editing method for introducing multiple programmed changes intoa single genomic locus in a single experiment.

SUMMARY

In one aspect, this application relates to a method for introducing aplurality of programmed nucleotide modifications into a single locus ofa desired genomic DNA sequence. The method entails the steps of: (a)synthesizing a homology-directed repair (HDR) library comprising aplurality of oligonucleotides, and (b) co-transfecting a population ofcells with (i) an expression system capable of expressing Cas9 and asingle guide RNA (sgRNA) and (ii) the HDR library, wherein theexpression system is capable of introducing the plurality ofoligonucleotides having the programmed nucleotide modifications to thelocus of the desired genomic DNA sequence in one or more cells of thepopulation. This method is carried out in a single experiment, i.e., ina single culture dish during a series of reactions carried out at thesame time or within a single experimental protocol. In step (a), eacholigonucleotide includes a programmed nucleotide modification in thelocus of the desired genome.

In some embodiments, each programmed nucleotide modification is a singlenucleotide variant. In some embodiments, the HDR library is constructedusing an oligonucleotide including a degenerate sequence and optionally,a selective PCR site. For example, the degenerate sequence is between 1and 100 nucleotides in length. In some embodiments, the HDR librarycontains a set of oligonucleotides having at least 100 unique programmednucleotide modifications, at least 200 unique programmed nucleotidemodifications, at least 300 unique programmed nucleotide modifications,at least 400 unique programmed nucleotide modifications, at least 500unique programmed nucleotide modifications, at least 600 uniqueprogrammed nucleotide modifications, at least 700 unique programmednucleotide modifications, at least 800 unique programmed nucleotidemodifications, at least 900 unique programmed nucleotide modifications,at least 1,000 unique programmed nucleotide modifications, at least3,000 unique programmed nucleotide modifications, at least 4,000 uniqueprogrammed nucleotide modifications, at least 5,000 unique programmednucleotide modifications, at least 6,000 unique programmed nucleotidemodifications, at least 7,000 unique programmed nucleotidemodifications, at least 8,000 unique programmed nucleotidemodifications, at least 9,000 unique programmed nucleotidemodifications, at least 10,000 unique programmed nucleotidemodifications, at least 12,000 unique programmed nucleotidemodifications, at least 14,000 unique programmed nucleotidemodifications, at least 16,000 unique programmed nucleotidemodifications, at least 18,000 unique programmed nucleotidemodifications, at least 20,000 unique programmed nucleotidemodifications, at least 25,000 unique programmed nucleotidemodifications, at least 30,000 unique programmed nucleotidemodifications, at least 40,000 unique programmed nucleotidemodifications, or at least 50,000 unique programmed nucleotidemodifications.

In some embodiments, the plurality of programmed nucleotidemodifications that are introduced to the locus of the desired genomicDNA sequence results in a saturating set of programmed nucleotidemodifications. In some embodiments, the plurality of oligonucleotidesare synthesized on a microarray. In other embodiments, the plurality ofoligonucleotides are synthesized in column-based synthesis.

In some embodiments, the plurality of oligonucleotides that aresynthesized as described above are used directly without any additionalamplification or cloning steps. Alternatively, the plurality ofoligonucleotides are amplified or cloned cloned to an HDR library beforebeing used to introduce programmed nucleotide modifications.

In some embodiments, the expression system includes a Cas9 expressioncassette that includes a nucleotide sequence which encodes a Cas9nuclease, an sgRNA expression cassette, and a species-specific promoterthat is specific to the population of cells.

In certain embodiments, each oligonucleotide of the HDR library includesa pair of homology arms.

In some embodiments, the method for introducing a plurality ofprogrammed nucleotide modifications into a single locus of a desiredgenomic DNA sequence further entails the steps of: (c) harvesting thepopulation of cells, (d) selectively amplifying a genomic DNA and RNAsample, wherein the edited sequences are amplified and the non-editedsequence are not amplified, and (e) sequencing the genomic DNA and RNAsample that has been selectively amplified, resulting in a set ofgenomic transcripts which include the plurality of programmed nucleotidemodifications. Optionally, the method further entails functionallyanalyzing the set of genomic transcripts using a functional assay. Forexample, the functional assay is selected from the group consisting oftargeted RNA sequencing to measure transcript abundance, targeted DNAsequencing to measure reduced cellular fitness, targeted chromatinimmunoprecipitation-sequencing (CHiP-seq) of co-activators to assayenhancers, increased cellular growth rate to assay cancer drivers ordrug resistance, and FACS-based phenotypic sorting for cellular assays.

In another aspect, this application relates to a method for analyzingthe functional consequence of a genomic mutation. The method entails thesteps of: (a) synthesizing a homology-directed repair (HDR) libraryincluding a plurality of oligonucleotides, wherein each oligonucleotidecontains a programmed nucleotide modification in the locus of thedesired genome, (b) co-transfecting a population of cells with (i) anexpression system capable of expressing Cas9 and a single guide RNA(sgRNA) and (ii) the HDR library, wherein the expression system iscapable of introducing the plurality of oligonucleotides having theprogrammed nucleotide modifications to the locus of the desired genomicDNA sequence in one or more cells of the population, (c) harvesting thepopulation of cells, (d) selectively amplifying a genomic DNA and RNAsample, wherein the edited sequences are amplified and the non-editedsequence are not amplified, (e) sequencing the genomic DNA and RNAsample that has been selectively amplified, resulting in a set ofgenomic transcripts which include the plurality of programmed nucleotidemodifications, and (f) functionally analyzing the set of genomictranscripts using a functional assay. This method is carried out in asingle experiment, i.e., during a series of reactions carried out at thesame time or within a single experimental protocol.

In some embodiments, the HDR library is constructed using anoligonucleotide containing a degenerate sequence and optionally, aselective PCR site. The degenerate sequence is between 1 and 100nucleotides in length. In some embodiments, the plurality ofoligonucleotides are synthesized on a microarray. In other embodiments,the plurality of oligonucleotides are synthesized in column-basedsynthesis. In some embodiments, the plurality of oligonucleotides areused directly without any cloning step to introduce programmednucleotide modifications. Alternatively, the plurality ofoligonucleotides are cloned to an HDR library before being used tointroduce programmed nucleotide modifications.

In some embodiments, the expression system includes a Cas9 expressioncassette having a nucleotide sequence which encodes a Cas9 nuclease, ansgRNA expression cassette, and a species promoter that is specific tothe population of cells

In some embodiments, each oligonucleotide of the HDR library comprises apair of homology arms.

In some embodiments, the functional assay is selected from the groupconsisting of targeted RNA sequencing to measure transcript abundance,targeted DNA sequencing to measure reduced cellular fitness, targetedchromatin immunoprecipitation-sequencing (CHiP-seq) of co-activators toassay enhancers, increased cellular growth rate to assay cancer driversor drug resistance, and FACS-based phenotypic sorting for cellularassays.

In another aspect, this application relates to a method for genomicscreening. The method entails the steps of: (a) introducing a pluralityof programmed nucleotide modifications to a single genomic locus,wherein the plurality of programmed nucleotide modifications areintroduced in a single experiment, i.e., during a series of reactionscarried out at the same time or within a single experimental protocol,(b) sequencing the genomic DNA or cDNA of the edited locus, and (c)quantifying the transcript abundance of each mutation.

In some embodiments, step (a) includes (1) synthesizing ahomology-directed repair (HDR) library comprising a plurality ofoligonucleotides, wherein each oligonucleotide includes a programmednucleotide modification in the locus of the desired genome, and (2)co-transfecting a population of cells with (i) an expression systemcapable of expressing Cas9 and a guide RNA (sgRNA) and (ii) the HDRlibrary, wherein the expression system is capable of introducing theplurality of oligonucleotides having the programmed nucleotidemodifications to the locus of the desired genomic DNA sequence in one ormore cells of the population. This step is carried out in a singleexperiment, i.e., during a series of reactions carried out at the sametime or within a single experimental protocol. In some embodiments, step(c) includes calculating an enrichment score for each mutation.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1 a-1 c show saturation genome editing and multiplex functionalanalysis of a hexamer region influencing BRCA1 splicing. FIG. 1 a is anexperimental schematic. Cultured cells were co-transfected with a singleCas9-sgRNA construct (CRISPR) and a complex homology-directed repair(HDR) library containing an edited exon that harbors a random hexamer(blue, green, orange) and a fixed selective PCR site (red).CRISPR-induced cutting stimulated homologous recombination with the HDRlibrary, inserting mutant exons into the genomes of many cells. At fivedays post-transfection, cells were harvested for gDNA and RNA. Afterreverse transcription, selective PCR was performed followed bysequencing of gDNA and cDNA derived amplicons. Hexamer enrichment scoreswere calculated by dividing cDNA counts normalized by gDNA counts. FIG.1 b shows correlation of enrichment scores between biological replicatesfor hexamers observed in each experiment with positions of previouslyidentified [9] exonic splicing enhancers (ESEs), exonic splicingsilencers (ESSs) and stop codons indicated. FIG. 1 c shows rank-orderedplot of enrichment scores with positions of ESEs, ESSs, and stop codonsindicated.

FIGS. 2 a-2 c show that multiplex homology-directed repair revealseffects of single nucleotide variants on transcript abundance. Threeseparate HDR libraries (R, R2, and L) containing a 3% mutation rate (97%wt, 1% each non-wt base) in either half of BRCA1 exon 18 were introducedto the genome via co-transfection with pCas9-sgBRCA1x18. Enrichmentscores were calculated for each haplotype observed at least 10 times inthe gDNA, and effect sizes of SNVs were determined by weighted linearregression modeling. ‘Sense’ includes both missense and synonymous SNVs.FIG. 2 a shows effect sizes calculated from replicate transfections ofHDR library R, consisting of a 3% per-nucleotide mutation rate in the3′-most 39 bases and the same selective PCR site used in FIG. 1, werehighly correlated (R=0.846). FIG. 2 b shows that Library R2 harbored aselective PCR site composed of 5 synonymous changes, none of which arepresent in Library R. When effect sizes derived from experiments withlibrary R2 were plotted against those from library R, there was a strongcorrelation (R=0.847), indicating reproducibility and demonstrating thatdifferences between selective PCR sites did not strongly influencescores. FIG. 2 c shows effect sizes for SNVs across the exon aredisplayed. Datasets from libraries R and L were combined to span theentire exon. Dashed lines represent SNVs that introduce nonsense codons.

FIGS. 3 a-3 c show saturation genome editing and multiplex functionalanalysis at an essential gene, DBR1, in Hap1 cells. An HDR librarytargeting a highly conserved region of DBR1 exon 2 was used withpCas9-EGFP-sgDbr1x2 to introduce point mutations across 75 base pair(bp) and all possible codon substitutions at three residues believed toparticipate at the enzyme's active site. FIG. 3 a shows that sequencingof gDNA from the HDR library and populations of edited cells at D5, D8,and D11 reveals selection for synonymous mutations, and depletion offrameshift, nonsense, and missense variants. FIG. 3 b shows that meanD11 enrichment scores are plotted as line segments for SNVs in the3′-most 73 bases of exon 2 and two bases of intron 2. Above theenrichment scores in ascending order are the wt nucleotide at eachposition, each one by genome edit, the wild-type amino acid (AA), andthe AA derived from each genome edit (asterisk indicates a stop codon).Segment color indicates mutation type, faded segments indicatediscordant effects between replicates, and AAs are colored according tothe Lesk color scheme (small nonpolar—orange, hydrophobic—green,polar—magenta, negatively-charged—red, and positively charged—blue). Thefirst nine bases shown correspond to the active site residues. FIG. 3 cshows that D8 and D11 amino acid level enrichment scores were calculatedfor active site residues N84, H85, E86 after excluding discordantobservations between replicates (FIG. 13 c). On both D8 and D11 strongselective effects and tolerance of only synonymous (green boxes) and afew missense variants were observed.

FIGS. 4 a-4 d show the distribution and pair-wise correlations ofhexamer abundances. FIG. 4 a shows the relative abundance of hexamerswithin the HDR library (top), gDNA (middle), cDNA data (bottom) areshown for a single experiment. The vertical black line represents ourthreshold of 10 gDNA reads. FIG. 4 b-4 d demonstrate that scatterplotsfrom a single replicate show pair-wise correlations between sequencingcounts for the HDR library, gDNA, and cDNA for hexamers with at least 10observations in the gDNA library, excluding wild type and controlhexamers (n=3,633). The HDR library and the gDNA data are most highlycorrelated (R 95% confidence interval (CI): 0.596-0.636), followed bythe gDNA and cDNA (R 95% CI: 0.419-0.471) and the HDR library and cDNA(R 95% CI: 0.341-0.394).

FIGS. 5 a-5 d show correlations for hexamer genome editing efficiencyand enrichment scores between replicates. FIG. 5 a shows that gDNAcounts for all hexamers with at least ten reads in each of two gDNApreps from separate transfections with the same HDR library (n=2,980)exhibited moderate correlation (R 95% CI: 0.355-0.416). FIG. 5 b showsthat hexamer editing rates, defined as gDNA counts normalized to HDRlibrary counts, were substantially less correlated (R 95% CI:0.084-0.155), consistent with a hexamer's HDR library abundancecontributing more to its gDNA abundance than systematic differences inHDR efficiency secondary to the hexamer sequence itself. FIG. 5 c showsthat hexamer enrichment scores for two pools of cells from a singletransfection split on D3 were well-correlated (R 95% CI: 0.643-0.681).FIG. 5 d shows that pooling data from cells split on D3 replicates froma single transfection yielded an improved correlation between biologicalreplicates (that is, independent transfections; R 95% CI: 0.690-0.722.

FIGS. 6 a-6 b show comparison of genome-based hexamer enrichment scoresto plasmid-based hexamer scores. FIG. 6 a shows that there was a modestcorrelation between ESS and ESE hexamers defined by a previous study [9](x-axis) and the enrichment scores calculated here (y-axis; Spearmanp=0.524). The previous study also interrogated hexamers positioned +5 to+10 nucleotides relative to a splice junction, but was plasmid-basedrather than genome-based and in the context of different exons. FIG. 6Bshows that to reveal effects of GC content on hexamer abundance,histograms display the distribution of enrichment scores for eachpossible G+C level (0-6). Hexamers containing two or fewer G+C basepairs exhibited broadly lower enrichment scores than hexamers containingthree or more G+C base pairs.

FIG. 7 shows experimental schematic for genome editing and functionalanalysis of BRCA1 exon 18. Cultured cells were co-transfected with asingle Cas9-sgRNA construct (CRISPR) and an HDR library. Each HDRlibrary was generated from cloning of an oligonucleotide synthesizedwith 3% nucleotide degeneracy (97WT:1:1:1) for approximately half of theexon and a selective PCR site introduced to the other (fixed) half ofthe exon (red). CRISPR-induced HDR integrates mutant exons into thegenome. Cells were cultured for five days post-transfection, and thenharvested for gDNA and total RNA. After reverse transcription, selectivePCR was performed before sequencing the edited pools of gDNA and cDNA.Each exon haplotype's enrichment score was measured by dividing cDNAreads by gDNA reads, and effect sizes for each SNV were calculated viaweighted linear regression.

FIGS. 8 a-8 c show positional SNV editing rates and replication ofeffect sizes. FIG. 8 a shows that editing rates for each SNV in BRCA1exon 18 were calculated by dividing each SNV's gDNA sequencing abundanceby its HDR library abundance. Editing rates were then plotted across theexon for each library (red=L, blue=R, green=R2) with locations of theirselective PCR sites and the CRISPR-targeted PAM illustrated below. ForHDR libraries R and R2, there was a subtle decrease in editing rate withincreasing distance from the Cas9 cleavage site (rho^(R)=−0.264,p^(R)=4.1×10⁻³; rho^(R2)=−0.361, p^(R2)=4.8×10⁻⁵). For library L, whichallowed re-cutting by not destroying the PAM, there was a sharp peak ofediting centered on the Cas9 cleavage site, and a rapid decline inefficiencies in the 5′ direction (further from the 3′ selective PCRhandle). FIGS. 8 b-8 c shows that SNV effect sizes were concordantacross biological replicates for libraries R2 (FIG. 8 b) and L (FIG. 8c) (library R shown in FIG. 2). Variants of high effect size scoredsimilarly across independent transfections.

FIG. 9 shows biological replicate effect size reproducibility for alllibraries. Three separate HDR libraries (R, R2, and L) containing 3%nucleotide degeneracy in either half of BRCA1 exon 18 were introduced tothe genome via co-transfection with pCas9-sgBRCA1x18. Enrichment scoreswere calculated for each haplotype observed at least ten times in thegDNA, and effect sizes of SNVs were determined by weighted linearregression. Effect sizes of individual variants for libraries R2 (left),R (middle), and L (right) were well correlated between biologicalreplicates. Dashed lines represent SNVs that introduce nonsense codons.

FIGS. 10 a-10 c show correlation between effect sizes and predicteddisruption of splicing motifs and indel effects. FIG. 10 a shows thatMutPred Splice [18] was used to predict the functional impact of all 234single nucleotide substitutions on splicing in BRCA1 exon 18 (x-axis),and these scores were compared to absolute values of the empiricallymeasured effect sizes (y-axis; p=0.322). Although nonsense variantscontributed to this trend, the sense variants with the largest effectsizes generally had high MutPred Splice scores. FIG. 10 b shows that forindels observed in gDNA from library 2 (virtually all of which occur atthe Cas9 cleavage site), size frequencies are plotted. Indel size=0includes all haplotypes with wild type length. FIG. 10 c shows that foreach indel size, enrichment scores were calculated and normalized tothat of the average full length exon. As predicted by nonsense-mediateddecay, indels that shift the coding frame were associated with lowtranscript abundance.

FIG. 11 shows experimental schematic for saturation genome editing andmultiplex functional analysis of DBR1 exon 2. Hap1 cells wereco-transfected with a single Cas9-2A-EGFP-sgRNA construct (CRISPR) andan HDR library cloned from array-synthesized oligonucleotides containingprogrammed SNVs (orange, blue) and active site codon substitutions(green). The HDR library exon haplotypes also included two synonymousmutations (red) to disrupt PAM and protospacer sequences to prevent Cas9re-cutting, and a 6 bp selective PCR site (light blue) substituted inthe downstream intron. Successfully transfected cells (EGFP+) wereselected on D2 by FACS, and cultured. On D5, D8, and D11, samples ofcells were taken and selective PCR was performed before targetedsequencing of gDNA. Each haplotype's enrichment score, a measure of thehaplotype's fitness in cell culture, was calculated by dividing D8 orD11 abundance by D5 abundance.

FIGS. 12 a-12 b show DBR1 editing rates by position and comparison ofhaplotype abundances between D5 and the HDR library, D8, and D11. FIG.12 a shows that editing rates for programmed SNVs represented in theDBR1 gDNA library above threshold (n=216) were calculated by normalizingeach SNV's gDNA abundance by its HDR library abundance. Rates areplotted by position, with the locations of the targeted PAM (orange) andselective PCR site (purple) indicated below. The editing rate did notsignificantly change with position (P>0.05), consistent with positionaleffects being negated by eliminating re-cutting and performing selectivePCR from a distal site. FIG. 12 b shows that scatterplots display thefrequencies at which each haplotype was observed in the D5 sample vs theHDR library, D8, and D11 samples. To account for bottlenecking fromediting of a limited number of cells in this representative experiment,analysis of individual haplotypes was restricted to those present atfrequencies above 5×10⁻⁵ in the D5 sample (n=377; represented by thevertical line). Selection was evident by the depletion of manyhaplotypes in D8 and D11 samples.

FIGS. 13 a-13 c show performance of computational predictions ofdeleterious DBR1 mutations and reproducibility between biologicalreplicates. FIG. 13 a shows that D11 enrichment scores from a singleexperiment were used to empirically define deleterious mutations asthose with scores fourfold below wild type (vertical line). FIG. 13 bshows that three in silico metrics of functional impairment were testedfor their ability to anticipate the deleteriousness of these mutationsas indicated by the area under the receiver operating characteristiccurve (AUC): BLOSUM62 [20] (AUC=0.672, 214 SNVs), PolyPhen-2 [21](AUC=0.671, 155 non-synonymous SNVs), and CADD [22] (AUC=0.701, 214SNVs). Despite the different approaches of these algorithms, all threeexhibited comparably moderate predictive power. FIG. 13 c shows that abiological replicate of the DBR1 experiment was performed and D11enrichment scores for amino acid substitutions were well correlated(grey lines on scatterplot indicate the ‘deleteriousness’ threshold offourfold depletion). The distribution of amino acid level enrichmentscores for each experiment is displayed along each axis, reflectingbimodality. Unexpected effects (that is, nonsense mutations scoring astolerated) were among the relatively small percentage of effects notconsistent between replicates.

DETAILED DESCRIPTION

Methods for introducing multiple programmed nucleotide modificationsinto a single locus of a desired genomic DNA sequence are providedherein. The methods described herein are carried out in a singleexperiment, i.e., during a series of reactions carried out concurrentlywithin a single experimental protocol in a single culture dish. Suchmethods may be used to analyze the functional consequence of a genomicmutation or for genomic screening.

To overcome the limitations of previously used methods, a method wasdeveloped to generate and functionally analyze hundreds to thousands ofprogrammed genome edits at a single locus in a single experiment. Themethod allows a more accurate and scalable measurement of the functionalconsequences of genetic variations. Measurement of the functionalconsequences of large numbers of mutations with saturation genomeediting potentially facilitates high-resolution functional dissection ofboth cis-regulatory elements and trans-acting factors, as well as theinterpretation of variants of uncertain significance observed inclinical sequencing.

According to the embodiments described herein, this application relatesto a method for introducing a plurality of programmed nucleotidemodifications into a single locus of a desired genomic DNA sequence.Saturation editing of genomic regions may be achieved by couplingCRISPR/Cas9 RNA-guided cleavage [10] with multiplex homology-directedrepair (HDR) using a complex library of donor templates. “Saturationediting” as used herein means that for a particular sequence, eachnucleotide position of that sequence is systematically modified witheach of all four traditional bases, A, T, G and C. For example, ahexamer substituted at each position would have 4,096 possible singlenucleotide variants (four possible substitutions at each of the sixnucleotide positions of the hexamer, or 4⁶=4,096).

The multiple programmed nucleotide modifications may be introducedduring a single experiment. The phrase “a single experiment” means thatmultiple programmed edits are introduced to a region of a particularsize within a single culture dish, during the course of one experimentor a series of reactions within a single experimental protocol. In otherwords, the programmed edits are introduced concurrently in a singleculture dish. In certain embodiments, the single experimental protocolincludes one or more concurrent reactions, i.e., the multiple programmededits are introduced at approximately the same time. This is in contrastto programmed edits being introduced one-by-one or several at a time inphysically separated reactions or experiments carried out using one ormore multi-well or otherwise separated culture dishes. The region to beintroduced with the programmed edits may have an optimal size thatallows efficient multiplex editing in one experiment, for example, theregion is about between 1 and 100 base pairs in size. The windowassociated with HDR mechanisms in mammalian cells [11] may affect thesize of the region that can be subjected to multiple editing in oneexperiment. Therefore, it is within the purview of one skilled in theart to determine the size of the region for multiplex editing. By thesame token, saturation genome editing of a full gene—e.g. to measurefunctional consequences of all possible variants of uncertainsignificance—will likely require multiple experiments tiling along itsexons.

The terms “programmed modifications,” “programmed gene edits,” and“programmed edits” as used herein are interchangeable, meaning that fora particular oligonucleotide, one or more nucleotides at a particularposition is changed, for example, from A to T, G, or C. In someembodiments, each programmed nucleotide modification or edit is a singlenucleotide variant (SNV). The programmed changes may result in adeletion, substitution, insertion, or other type of mutation to thegene.

The method includes a step of synthesizing a homology-directed repair(HDR) library comprising a plurality of oligonucleotides, each of whichincludes a programmed nucleotide modification. The plurality ofoligonucleotides may be synthesized on a microarray or in column-basedsynthesis. In some embodiments, the HDR library is constructed using anoligonucleotide having a degenerate sequence and optionally, a selectivePCR site.

The degenerate sequence may be between 1 and 100 nucleotides in length,and the constructed library using the degenerate sequence may have a setof oligonucleotides having at least 100 unique programmed nucleotidemodifications, at least 200 unique programmed nucleotide modifications,at least 300 unique programmed nucleotide modifications, at least 400unique programmed nucleotide modifications, at least 500 uniqueprogrammed nucleotide modifications, at least 600 unique programmednucleotide modifications, at least 700 unique programmed nucleotidemodifications, at least 800 unique programmed nucleotide modifications,at least 900 unique programmed nucleotide modifications, at least 1,000unique programmed nucleotide modifications, at least 3,000 uniqueprogrammed nucleotide modifications, at least 4,000 unique programmednucleotide modifications, at least 5,000 unique programmed nucleotidemodifications, at least 6,000 unique programmed nucleotidemodifications, at least 7,000 unique programmed nucleotidemodifications, at least 8,000 unique programmed nucleotidemodifications, at least 9,000 unique programmed nucleotidemodifications, at least 10,000 unique programmed nucleotidemodifications, at least 12,000 unique programmed nucleotidemodifications, at least 14,000 unique programmed nucleotidemodifications, at least 16,000 unique programmed nucleotidemodifications, at least 18,000 unique programmed nucleotidemodifications, at least 20,000 unique programmed nucleotidemodifications, at least 25,000 unique programmed nucleotidemodifications, at least 30,000 unique programmed nucleotidemodifications, at least 40,000 unique programmed nucleotidemodifications, or at least 50,000 unique programmed nucleotidemodifications.

The method further includes a step of co-transfecting a population ofcells with (i) an expression system capable of expressing Cas9 and aguide RNA (sgRNA) and (ii) the HDR library. In such embodiments, theexpression system acts to introduce a plurality of oligonucleotides(each of which includes a programmed nucleotide modification) to thelocus of the desired genomic DNA sequence in one or more cells of thepopulation. In certain embodiments, the expression system includes aplasmid which includes a Cas9 expression cassette that includes anucleotide sequence which encodes a Cas9 nuclease, an sgRNA expressioncassette, and a species-specific promoter that is specific to thepopulation of cells. In certain aspects, each oligonucleotide member ofthe HDR library includes a pair of homology arms in order to target thedesired genomic DNA sequence.

The method described herein may further include one or more steps ofharvesting the population of cells after culturing the transfectedcells, selectively amplifying a genomic DNA and RNA sample wherein theedited sequences are amplified and the non-edited sequence are notamplified, and sequencing the genomic DNA and RNA sample that has beenselectively amplified, resulting in a set of genomic transcripts whichinclude the plurality of programmed nucleotide modifications. In someembodiments, the method includes functionally analyzing the set ofgenomic transcripts using a functional assay, such as targeted RNAsequencing to measure transcript abundance, targeted DNA sequencing tomeasure reduced cellular fitness, targeted chromatinimmunoprecipitation-sequencing (CHiP-seq) of co-activators to assayenhancers, increased cellular growth rate to assay cancer drivers ordrug resistance, and FACS-based phenotypic sorting for cellular assays.

In one aspect, this application also relates to analyzing the functionalconsequence of a genomic mutation by carrying out the above steps,including: (a) synthesizing a homology-directed repair (HDR) librarycomprising a plurality of oligonucleotides, wherein each oligonucleotidecomprises a programmed nucleotide modification in the locus of thedesired genome; (b) co-transfecting a population of cells with (i) anexpression system capable of expressing Cas9 and a guide RNA (sgRNA) and(ii) the HDR library, wherein the expression system is capable ofintroducing the plurality of oligonucleotides having the programmednucleotide modifications to the locus of the desired genomic DNAsequence in one or more cells of the population; (c) harvesting thepopulation of cells; (d) selectively amplifying a genomic DNA and RNAsample, wherein the edited sequences are amplified and the non-editedsequence are not amplified; (e) sequencing the genomic DNA and RNAsample that has been selectively amplified, resulting in a set ofgenomic transcripts which include the plurality of programmed nucleotidemodifications; and (f) functionally analyzing the set of genomictranscripts using a functional assay.

In some embodiments, the functional assay is biologically relevant andtechnically viable. In some embodiments, the functional assay directlylinks genotype to phenotype. For example, the functional assay is atargeted RNA sequencing to measure transcript abundance or targeted DNAsequencing to measure reduced cellular fitness. In other embodiments,the functional assay is targeted ChIP-seq of co-activators to assayenhancers, increased cellular growth rate to assay cancer drivers ordrug resistance [31], or FACS-based phenotypic sorting for cellularassays [32].

Also described herein is a method for genomic screening. The methodincludes a first step of introducing a plurality of programmednucleotide modifications to a single genomic locus, for example, asdescribed above. The genomic screening method further includessequencing the genomic DNA or cDNA of the edited locus, and quantifyingthe transcript abundance of each mutation, e.g., by calculating anenrichment score for each mutation.

For illustration purposes, the saturation genome edits were introducedto exon 18 of BRCA1 and to a well-conserved coding region of anessential gene, DBR1, respectively. By no means the scope of thisapplication is limited to these particular genes. It is within thepurview of one skilled in the art to introduce genome edits includingsaturation genome edits to any gene of interest by carrying out themethods disclosed herein.

In exon 18 of BRCA1, a six base-pair (bp) genomic region was replacedwith all possible hexamers, or the full exon was replaced with allpossible single nucleotide variants (SNVs), and the effects ontranscript abundance attributable to nonsense-mediated decay and exonicsplicing elements were measured. Saturation genome edits were introducedto DBR1 in a similar fashion and the relative effects on growth thatcorrelate with functional impact were measured.

In one embodiment, the methods described herein are exemplified byleveraging CRISPR/Cas9 [10, 12, 13] to introduce saturating sets ofprogrammed edits to a specific locus via multiplex HDR. As illustratedin FIG. 1 a, six bases of a BRCA1 exon are targeted [14] by cloning anHDR library containing random hexamers substituted at positions +5 to+10 of BRCA1 exon 18 and fixing nonsynonymous changes at positions +17to +23 (as a ‘handle’ for selective PCR and to prevent re-cutting [15]by destroying the protospacer adjacent motif (PAM)). The oligonucleotidesequences used are shown in Table 1.

pCas9-sgBRCA1x18 and the HDR library were co-transfected into ˜800,000HEK293T cells, achieving 3.33% HDR efficiency. Two independenttransfections were performed with the same HDR library (biologicalreplicates' 1, 2), and cells were split on day 3 (‘D3 replicates’ a, b).

Genomic DNA (gDNA) and cDNA from bulk cells on D5 were prepared. PCRreactions were primed on the ‘handle’ uniquely present withinsuccessfully edited genomes. Amplification was observed in HDRlibrary/pCas9-sgBRCA1x18 transfected samples, but not in HDRlibrary-only controls. Amplicons derived from gDNA and cDNA were deeplysequenced (FIG. 1 a). The relative abundances of hexamers withinreplicates and the correlation between the HDR library and edited gDNAwere consistent with limited ‘bottlenecking’ during transfection andminimal influence of hexamer identity on HDR efficiency (FIG. 4 and FIG.5).

The effect of introducing each hexamer to these genomic coordinates ontranscript abundance was estimated by calculating enrichment scores(cDNA divided by gDNA counts, calibrated to wild-type). These enrichmentscores were well correlated between biological replicates (FIG. 1 b, 1avs. 2a: R=0.659) and between D3 replicates (FIG. 5 c; 1a vs. 1b:R=0.662). Correlation between biological replicates improved when readcounts were pooled from D3 replicates (FIG. 5 d; 1 vs. 2: R=0.706).

To maximize precision, data across all four replicates for 4,048hexamers were merged (FIG. 1 c; Table 2). Several results support thebiological validity of the resulting enrichment scores. First, aspredicated by nonsense-mediated decay (NMD), hexamers introducing stopcodons were associated with markedly reduced mRNA levels (FIG. 1 c;Wilcoxon rank sum test (WRST) P=9.7×10-84; median for nonsense hexamers12-fold below overall median). Second, previous studies measured hexamerinfluence on splicing at analogous coordinates of different exons via aplasmid minigene assay [9]. Despite these contextual differences, thestrongest exonic splicing silencers (ESSs) (bottom 2% in ref [9]) scored9-fold below median (FIG. 1 c; WRST P=2.0×10-24), the strongest exonicsplicing enhancers (ESEs) (top 2% in ref 14) scored 1.5-fold abovemedian (FIG. 1 c; WRST P=2.4×10-11), and the complete datasetscorrelated reasonably well (FIG. 6 a; p=0.524). Correlation between GCcontent and enrichment scores was also observed (FIG. 6 b), strongestfor bases most proximal to the splice junction, consistent with aposited role for GC content in the stability of splicing structures [16](although reverse transcription bias is a potential confounder).

In some embodiments, FIG. 7 illustrates the assay of the effects of SNVsacross the full 78 bp BRCA1 exon 18. Three HDR libraries were clonedwith selective PCR sites in either the 5′ or 3′ region and 3% doping[17] (97 (wt):1:1:1) in the other half of the exon (L: 5′ degeneracy, 3′nonsynonymous selective PCR site; R: 3′ degeneracy, 5′ nonsynonymousselective PCR site; R2: 3′ degeneracy, 5′ synonymous selective PCR site)(Table 1). Five days post-transfection with pCas9-sgBRCA1x18 (1.02-1.29%HDR efficiency), gDNA and cDNA were selectively amplified and deeplysequenced.

Using data from all edited exons with ≧1 mutation and ≧10 gDNA counts,effect sizes (beta values) of all possible SNVs were estimated using aweighted linear model. Estimated effect sizes were reproducible (R=0.846(R), 0.853 (R2), and 0.686 (L); FIG. 2 a, FIGS. 8-9, Table 3). Effectsizes for the same SNVs interrogated with different selective PCRstrategies (R vs. R2) were also well correlated (R=0.847; FIG. 2 b).

The estimated effect sizes reflect empirically measured changes intranscript abundance resulting from programmed edits (FIG. 2 c). Aspredicted with NMD, nonsense mutations reduced transcript abundance(WRST P=1.4×10−203; 5.6−fold below median). Additionally, severalmissense and synonymous SNVs reproducibly resulted in large reductionsin transcript abundance, and SNV effect sizes correlated with apredictive model for exonic variants that disrupt splicing [18](p=0.322; FIG. 10 a). Because library L does not destroy the PAM,enrichment scores for indels were calculated from non-homologousend-joining (NHEJ). As predicted with NMD, only frameshifting indelswere associated with large depletions (FIGS. 10 b, 10 c).

In another embodiment, FIG. 11 illustrates targeting a well-conservedregion of DBR1, the RNA lariat debranching enzyme, which scored highlyin a genome-wide screen for essentiality [19]. Array-synthesizedoligonucleotides were used to program a DBR1 HDR library to include thewild-type sequence and every possible SNV across 75 bp (73 3′-most basesof exon 2 and first two bases of intron 2), and also all 63 possiblecodon substitutions at three residues (388 genome edits were programmed;single base deletions were abundant from synthesis errors). The HDRlibrary also introduced two fixed synonymous changes (to disrupt the PAMand prevent re-cutting [15]) and a selective PCR site in intron 2.

An optimized single guide RNA (sgRNA) sequence [23, 24] was cloned intoa bicistronic sgRNA/Cas9-2A-EGFP vector (pCas9-EGFP-sgDbr1x2). Fivemillion haploid human cells [25] (Hap1) were co-transfected with theDBR1 HDR library and pCas9-EGFP-sgDbr1x2. On D2, ˜250,000 EGFP+ cellswere FACS sorted and further cultured, taking samples on D5, D8 and D11(1.14% HDR efficiency, estimated on D8). Following gDNA isolation andselective PCR, deep sequencing was performed to quantify the relativeabundance of edited haplotypes in each sample.

The relative proportions of mutation classes at each time point werefirst examined (FIG. 3 a). The strong enrichment of synonymous mutationsand depletion of nonsense and frameshifting mutations over timeindicated that selection was acting on edited cells in culture,consistent with DBR1 essentiality. The enrichment scores (D8 or D11counts divided by D5 counts) for 365 of the 388 (94%) programmed editsand 12 single base deletions (the subset with relative abundance >5×10-5on D5) were calculated (FIG. 3 b; FIG. 12; Table 4). Enrichment scoresstrongly correlated with functional consequence. The median enrichmentscore for synonymous edits was nearly identical to wild-type (1.006-foldlower), but 73-fold lower for missense edits (P=1.7×10-8; WRST againstsynonymous edits), 207-fold lower for nonsense edits (P=1.9×10-9), and211-fold lower for frameshifting single base deletion edits(P=1.5×10-8). Furthermore, enrichment scores for SNVs were inverselycorrelated with metrics of predicted deleteriousness like CADD [22](p=−0.295; P=1.2×10-5; FIGS. 13 a, 13 b). Residues N84, H85 and E86 ofDBR1 were edited to all 63 possible non-wild-type codons. Consistentwith their predicted role in the active site of an essential enzyme[26], only synonymous mutations and a few missense substitutions weretolerated (FIG. 3 c).

Amino-acid level enrichment scores were well correlated between D11biological replicates (R=0.752; P=2.6×10-40; FIG. 13 c), and werebimodally distributed in each replicate, allowing broad classificationof changes as tolerated or deleterious. The small proportion ofdiscordantly classified variants might be explained by Hap1 reversion todiploidy or off-target effects, highlighting the importance ofbiological replicates for this experimental design. There were noreproducibly tolerated nonsense or frameshifting edits. These dataindicate that the empirically derived enrichment scores reflect truebiological effects of specific genomic point mutations within DBR1.

Genome editing efficiency may be affected by factors such asbottlenecking complexity, limiting reproducibility and in some cases,necessitating the optional selective PCR sites. However, selective PCRsites are not necessarily required in all cases. In some embodiments, avariety of techniques, e.g. transient hypothermia [27] oroligonucleotide-based HDR [28], can be used to improve editingefficiency. In some embodiments, ZFNs and TALENs may improveefficiencies up to 50% [29, 30].

In some embodiments, haploid cells for DBR1 mutagenesis can be used toimprove editing efficiency. In other embodiments, mutagenesis can beperformed in diploid cells by knocking out one allele via NHEJ and thenknocking in the HDR library to the other allele.

The following examples are intended to illustrate various embodiments ofthe invention. As such, the specific embodiments discussed are not to beconstrued as limitations on the scope of the invention. It will beapparent to one skilled in the art that various equivalents, changes,and modifications may be made without departing from the scope ofinvention, and it is understood that such equivalent embodiments are tobe included herein. Further, all references cited in the disclosure arehereby incorporated by reference in their entireties, as if fully setforth herein.

Examples BRCA1 Experimental Design

An exon in a clinically relevant gene in which known mutations causeaberrant splicing was chosen to be targeted. Previous molecular studiesof a G to T nonsense mutation occurring naturally in cancer patients atchr17:41,215,963 suggested exon skipping [14] was secondary to thecreation of an exonic splicing silencer site [33]. It is hypothesizedthat saturation genome editing of this exon could result in a wide rangeof splicing outcomes.

When performing parallel functional analysis of complex allelic series,how to associate each of many mutations with the biological effects theyproduce should be considered. It is more difficult when attempting suchapproaches at the endogenous genomic locus, and with limited editingefficiencies. By performing these experiments in an exon and focusing onthe effects of mutations on transcript abundance, genotype and phenotypeare directly linked by observing the frequency of each genome edit inthe transcript pool, relative to its frequency in genomic DNA. Thisdesign is advantageous because it requires no specialized (i.e.gene-specific) functional assay, thus making it amenable tointerrogation of transcribed variants' effects on splicing/transcriptabundance in any gene.

Inclusion of Selective PCR Sites

Given the modest proportion of HDR-edited loci in a given experiment andthe high number of variants to be interrogated (i.e. hundreds tothousands), it would require a large amount of sequencing tosufficiently sample every variant in gDNA and cDNA pools from apopulation of cells that are predominantly unedited or harboringproducts of NHEJ. Furthermore, at such efficiencies, the rate of errorin high-throughput sequencing is high enough to obscure signal fromsingle nucleotide variants (SNVs) (unpublished observations). Therefore,in certain embodiments, until better methods are developed, techniquesto selectively sequence molecules derived from edited cells are likelyto be advantageous to isolate populations of cells that have beensuccessfully edited with HDR techniques. In some embodiments, selectivePCR sites are present regardless how the HDR libraries are generated,for example, by degenerate oligonucleotide or by programmed edits viamicroarray-based synthesis. In other embodiments, selective PCR sitesare not used.

The HDR libraries were designed to include short, fixed edits to serveas unique priming sites in genomes that successfully undergo HDR. PCRreactions primed at this site, therefore, should only amplify materialfrom edited cells, thus reducing both the noise associated with errorfrom sequencing unedited material and the cost of sequencing in eachexperiment. Additionally, selective PCR sites that mutate the PAM andprotospacer sequences could prevent Cas9 from re-cutting HDR-editedgenomes. This should have the effect of increasing the proportion ofcells bearing experimentally informative edits, and given the bottleneckimposed by limitations on how many successfully edited cells can besampled, should result in more robust experimental signal.

DBR1 Experimental Design

To demonstrate that saturation genome editing can be used to exploreeffects of mutations on protein function and cellular fitness, DBR1, awell-conserved gene that scored highly in a human haploid cellgenome-wide loss-of-function screen for essentiality [19] was targeted.Using haploid cells prevents gene compensation from an unedited copy[25]. Without knowing how sensitive the cells would be to mutations, itwas chosen to target a region of exon 2 that was highly conserved,included in all transcript annotations on the UCSC Genome Browser, andcoded for at least 2 residues (N84, H85) predicted to participate at theenzyme's active site [26]. Selection against edited cells in cultureallows phenotype to be linked to genotype from sequencing of the gDNApool over a series of time points. During HDR library construction, aselective PCR site in a downstream intron was designed to minimize anyeffect on gene function, and two synonymous mutations to abrogate Cas9re-cutting were used.

Given the lower transfection efficiency of Hap1 cells (˜4% for theplasmids used here), a DBR1-targeting CRISPR construct that expressedEGFP with Cas9 was cloned and FACS was used to sort a population ofsuccessfully transfected cells. The sgRNA was designed using the ZhangLab tool [described at http://crispr.mit.edu/], and selected to minimizeoff-target effects that could potentially impair cellular fitness [23].

HDR Library and Cas9-sgRNA Cloning

A homology-directed repair (HDR) library containing all possible 4,096DNA hexamers substituted at positions +5 to +10 of BRCA1 exon 18(chr17:41,215,962-41,215,967; CCDS11453.1) was constructed using apartially degenerate oligonucleotide (IDT DNA; “BRCA1ex18NNNNNN5_(—)10selPCR”) containing a 7 bp selective PCR site/EcoRV restriction digestsite at position +17 to +23 (FIG. 1 a, Table 1). The oligonucleotide wasPCR amplified and cloned via the In-Fusion reaction (Clontech) into aPCR-linearized pUC19-BRCA1ex18 vector containing a pre-inserted 1,573 bpfragment amplified from the surrounding BRCA1ex18 locus in HEK293T cells(chr17:41,215,127-41,216,699) to serve as homologous arms. Additionallibraries from a second degenerate oligonucleotide that was synthesizedwith a 3% mutation rate (97% wt, 1% each non-wt base) across the 78 bpexon were cloned similarly, such that one end of the exon would be fixedand contain either missense (as above) or synonymous mutations forselective PCR. Complete oligonucleotide and HDR library exon sequencesare listed in Table 1. All PCR reactions were performed with the KAPAHiFi HotStart ReadyMix PCR Kit.

The DBR1 HDR library was cloned as above except with the followingdifferences. HDR library variants were derived from 388 oligonucleotidessynthesized on a microarray (CustomArray) to include all possible singlebase pair changes in a 75 bp region comprising part of DBR1 exon 2(chr3:137,892,342-137,892,416), all codon variants at the first threeresidues of the 75 bp region (chr3:137,892,408-137,892,416), and thereference 75 bp sequence. All DBR1 HDR library sequences also includedtwo synonymous mutations designed to prevent re-cutting of editedgenomes by disrupting PAM and protospacer sequences (chr3:137,892,424and chr3:137,892,421), and a 6 bp selective PCR site in intron 2 of DBR1(chr3:137,892,331-137,892,336). The library was cloned into apUC19-DBR1ex2 backbone, a vector containing the surrounding DBR1sequence cloned from Hap1 gDNA (chr3:137,891,573-137,893,293).

A bicistronic Cas9-sgRNA vector designed to cleave within BRCA1 exon 18(“pCas9-sgBRCA1x18”) was cloned according to a published protocol[24] byligating annealed oligonucleotides into a human codon-optimized S.pyogenous Cas9-sgRNA vector from the lab of Feng Zhang(pX330-U6-Chimeric_BB-CBh-hSpCas9; Addgene plasmid #42230). The sameprotocol was followed to create pCas9-EGFP-sgDbr1x2 from a similar Zhanglab vector that allows for fluorescent identification of Cas9-expressingcells (pSpCas9(BB)-2A-GFP (pX458); Addgene plasmid #48138).

Cell Culture and Transfection

For BRCA1 experiments, HEK293T cells were cultured in Dulbecco'sModified Eagle Medium (Life Technologies) supplemented with 10% FBS(AATC) and 100 U/ml penicillin+100 ug/ml streptomycin (LifeTechnologies). One day prior to transfection, cells were split to ˜40%confluency in 12-well plates with antibiotic-free media. The next day,0.5-1.0 ug of each library was co-transfected (Lipofectamine 2000,Invitrogen) with an equivalent amount of pCas9-sgBRCA1x18. Cells wereexpanded to 6-well plates, then split 1:4 on day 3 into two pools, andDNA and RNA were harvested on D5 (AllPrep DNA/RNA Mini Kit, Qiagen).Biological replicates of each transfection and negative controltransfections of each library without pCas9-sgBRCA1x18 were alsoperformed.

For the DBR1 experiment, Hap1 cells (Haplogen) were cultured in Iscove'sModified Dulbecco's Medium supplemented with 10% FBS and 100 U/mlpenicillin+100 ug/ml streptomycin. ˜3×10⁶ Hap1 cells were passaged to a60 mm dish in antibiotic-free media one day prior to co-transfectionwith 3 ug each of pCas9-EGFP-sgDbr1x2 and the DBR1 HDR library viaTurbofectin 8.0 (OriGene) according to protocol. On D2, FACS wasperformed (BD FACSAria III) to isolate ˜250,000 EGFP+ cells, which werethen expanded in culture with samples taken of ˜1×10⁶ cells on D5, and4-8×10⁶ on D8 and D11. gDNA was isolated according to protocol with theQiaAmp Kit (Qiagen). A biological replicate was performed, as well asnegative controls in which the HDR library was transfected with theempty pSpCas9(BB)-2A-GFP construct (to enable FACS of transfected cellswithout editing).

RT, Selective PCR and Sequencing

For BRCA1 experiments, reverse transcription (RT) was performed usingSuperScriptIII (Invitrogen) with a gene-specific primer located ineither BRCA1 exon 19 (hexamer experiments) or exon 21 (whole exonexperiments). Initial rounds of PCR were performed on large quantitiesof sample gDNA (8-12 ug gDNA, 100-150 ng/reaction) and cDNA (25 ug totalRNA reverse transcribed and split into 45-47 reactions) using the KAPAHiFi HotStart ReadyMix PCR kit. In the first gDNA PCR, a primer externalto the HDR library was used to prevent amplification of plasmid DNA.cDNA reactions were either primed from exons 16 and 18 (hexamerexperiment; Library L) or exons 18 and 20 (Libraries R, R2). After theinitial gDNA and cDNA reactions, all PCR products from a single samplewere pooled and purified using the QIAquick PCR Purification Kit(Qiagen).

For both cDNA and gDNA reactions, a primer designed to selectivelyamplify edited molecules bearing the selective PCR site was used eitherin the first or second reaction. Optimal annealing temperatures for eachprimer pair were determined via gradient PCR, and negative controlreactions were performed using input from HDR library-only transfectionsto ensure products were derived from edited genomes as opposed to theHDR library. Negative controls failed to amplify for all experiments.Two subsequent PCRs were performed to add sequencing adaptors (“PU1L”and “PU1R”), sample indices, and flow cell adaptors.

For the DBR1 experiment, 30 cycles of selective PCR were performed ongDNA (300 ng per reaction) from D5 (3 ug), D8 and D11 (27 ug each).Wells from each sample were pooled, PCR purified, and then re-amplifiedfor 15 additional cycles. The 1,055 bp product was gel-purified(QIAquick Gel Extraction Kit, Qiagen), and two subsequent PCRs wereperformed to incorporate sequencing and flow cell adaptors prior tosequencing as above.

After final reactions were purified (AMPure XP beads, Agencourt),paired-end sequencing was performed on all samples with the IlluminaMiSeq to quantify gDNA and/or cDNA abundances for each edited haplotype.All primer sequences for RT, selective PCR, and sequencing librarypreparation are provided in Table 1.

HDR efficiencies were estimated for all experiments via deep sequencingof target loci by performing PCR on 150-300 ng of gDNA using primersexternal to the region of editing and the selective PCR site. ReportedHDR efficiencies were conservatively calculated as the fraction ofsequencing reads containing the selective PCR site and bearing at leastone variant represented in the HDR library.

Analysis of Sequencing Data

For quality control, fully overlapping paired-end reads were merged withPEAR [34] (Paired-End reAd mergeR) and discordant pairs were eliminated.By design, the mutagenized region is covered by both the forward andreverse reads on the Illumina platform, resulting in high-confidencecalls per site.

For BRCA1 hexamer reads to be included, the six bases on either side ofthe hexamer were required to match the reference sequence, and everybase call in the hexamer required a quality score of at least Q30. ForBRCA1 whole-exon mutagenesis, the full read was required to be thecorrect length and match the library consensus sequence outside of themutagenized region, every base quality score inside the mutagenizedregion was required to be at least Q30, and no indels were tolerated inalignment with BWA-MEM [35]. cDNA reads not matching any gDNA haplotypewith at least 10 reads were eliminated. After normalizing for sequencingcoverage, enrichment scores were calculated as cDNA read countsincremented by one pseudocount divided by gDNA reads, calibrated to thewild-type hexamer.

For DBR1 mutagenesis, reads were subjected to the same requirements ofthe sequence outside the mutagenized bases matching the consensus andevery quality score in the mutagenized region exceeding Q30. Only readsmatching programmed haplotypes were analyzed, and haplotypes below a D5relative abundance of 5E-5 were excluded from analysis. Afterincrementing all read counts by one pseudocount and dividing by thetotal number of reads, the abundance of each haplotype on D8 or D11 wasdivided by the corresponding abundance on D5, and the fold changerelative to the wild type sequence was taken to calculate an enrichmentscore. Based on the bimodal distribution observed in each replicate,mutations with log₂-transformed enrichment scores less than −2 wereconsidered “deleterious”; otherwise, mutations were considered“tolerated”. Discordant effects between replicates were defined asmutations “tolerated” in one replicate but “deleterious” in the other.Amino acid level enrichment scores were calculated as the median of SNVenrichment scores for programmed edits resulting in the same change (orlack of change, for synonymous edits).

SNV Effect Size Linear Modeling and Replicate Pooling

To determine effects of SNVs in the BRCA1 whole-exon experiments, cDNAand gDNA read counts were converted into percentages (number of readsfor a given haplotype divided by the total number of reads for a givenreplicate) after discarding haplotypes with fewer than 10 gDNA reads.Because we had variance in the number of reads for each haplotype, thenull expectation of equal variance (σ2) for each cDNA/gDNA ratio wasviolated. Because each effect size (yij) was the average of nijobservations (reads), then var(yij)=var εij=σ2/nij, suggesting that theweight for each variable should be nij. To predict single nucleotideeffect size across exon 18 of BRCA1, we then fit the weighted linearmodel:

y _(ij)=β₀ +w _(ij)β_(ij) X _(ij)

where y_(ij) is the log₂ enrichment score for a given haplotype, is thenumber of gDNA reads for a given haplotype, β_(ij) is the effect ofnucleotide i at position j relative to the wild-type allele, and X_(ij)is a dummy variable indicating the presence or absence of a particularnucleotide change i at position j relative to the wild type allele.Regression analyses were performed in R 3.0.0 using the lm( ) function.The resulting coefficients of the model adjusted for the modelintercepts (β₀+β_(ij)) were taken as effect sizes of the individual SNVson exon splicing/stability. To merge data across replicates, effectsizes were averaged (including across overlapping bases betweenlibraries L and R in BRCA1 exon).

Comparisons to Other Metrics of Functional Impact

For comparison to plasmid studies, ESR-seq scores were taken from Ke etal. (2011) [9]. Hexamers with positive ESR-seq scores are deemed exonicsplicing enhancers, whereas negative ESR-seq scores denote exonicsplicing silencers. For comparison of BRCA1 exon 18's SNV effect sizesto an in silico method, all SNVs were queried on MutPredSplice's webserver (http://mutdb.org/mutpredsplice/submit.htm). MutPredSplicereports a single score estimating the likelihood that a variant willdisrupt splicing at any genomic locus. Absolute values of BRCA1 exon 18splicing effect sizes were then correlated with MutPredSplice scores todetermine concordance between our data and predicted effects onsplicing.

For DBR1, calculated enrichment scores were compared to BLOSUM62substitution scores [20] (obtained from NCBI), PolyPhen-2 [21], and CADD[22] (PolyPhen-2 and CADD scores obtained from querying genomiccoordinates from CADD's precomputed genomic annotations(http://cadd.gs.washington.edu/download). Whereas BLOSUM62 is derivedfrom evolutionary conservation and PolyPhen-2 predicts changes inprotein function, CADD is an integrated measure of deleteriousness thatincorporates many functional annotations (including PolyPhen-2).

Discussion

Reproducibility of Saturation Genome Editing Experiments

The correlations between replicates for each of the experiments suggestthat while this technique reproducibly measures effects of manyconcurrent programmed genome edits, there are also sources of noise.

The noise observed may relate to the fact that modest editingefficiencies lead to relatively few cells in each experiment harboringeach specific edit. In the BRCA1 hexamer experiment and the DBR1experiment, a bimodal distribution of gDNA read counts is observed(FIGS. 4 a, 12 b). This is consistent with a bottleneck resulting in notall HDR library edits being present in post-editing gDNA. If some editsare not present at all, some edits may be only made once or a few times,and may be represented by very few cells when measurements are made,possibly as few as one.

Consistent with lowly sampled edits being more prone to noise, hexamersthat are more highly represented in gDNA counts are more reproducible.For example, whereas R=0.659 between two biological replicates overall,hexamers falling into the top third with respect to gDNA countcorrelated much more highly (R=0.857). Furthermore, considering the twoBRCA1 experiments, because there were far fewer possible SNVs (n=234;experiment in FIG. 2) than hexamer substitutions (n=4,095; experiment inFIG. 1), each individual edit is expected to be created independentlymany more times during editing, given a generally similar experimentalsetup with respect to number of cells, functional assay, etc. This maygive rise to the higher reproducibility of the SNV effect sizes ascompared with the hexamer enrichment scores (i.e. FIG. 2 a vs. FIG. 1b).

Whether the noise represents biological variability (for instance, twocells with the same edit producing transcripts at different rates) ortechnical variability (stochastic effects inherent to sample prep) it isreasoned that by pooling or averaging replicates, the number ofsuccessfully edited cells sampled is effectively increased, andtherefore noise attributable to low sampling is reduced. Consistent withthis, pooling read counts from D3 replicates in the BRCA1 hexamerexperiment improved correlation between biological replicates.

For the DBR1 experiment, the overall reproducibility of D11 enrichmentscores is reasonable (R=0.752; FIG. 13 c). In each biological replicate,a bimodal distribution of enrichment scores (i.e. corresponding totolerated vs. deleterious) is observed. While there are someobservations, e.g. nonsense mutations that are tolerated in onereplicate, not all of the observations replicated. While two synonymouschanges score as reproducibly deleterious, there are no nonsense orframeshift mutations that are reproducibly tolerated.

This experiment, subject to bottlenecking at the editing step, generatesclonal populations possibly expanded from a single edited cell. Falselytolerated edits (i.e. nonsense mutations not selected against) in agiven replicate could be explained by Hap1 cells' reversion to diploidyprior to editing occurring, as noted by Haplogen (the cell line'ssource). Falsely deleterious edits in a given replicate could beobserved due to off-target CRISPR cutting in other essential regions, orrandom dropout when half the sample is split on D5.

These findings suggest that while the technique is sensitive enough tomeasure effects from very few edited cells, noise associated withsampling such small populations mandates the necessity of replicatingdata sets to improve confidence in the measurements associated withindividual genome edits. The data also suggest that increasedreproducibility may be achievable by a) transfecting and analyzing ahigher number of cells, b) limiting complexity of HDR libraries, or c)improving HDR efficiency to allow for sampling of more edited cells.

Potential Applications of Saturation Genome Editing

In the experiments disclosed herein, genotype is directly linked tophenotype to assay pools of multiplex HDR-derived variants. Targeted RNAand DNA sequencing of the edits themselves via selective PCR are wellsuited to catalog variants' effects on splicing and cellular fitness,respectively. However, with relatively simple adaptations of the method,complex pools of genome edits can be subjected to many additional assaysthat measure diverse aspects of biology.

First, the approach illustrated in the BRCA1 experiments is broadlyapplicable to study how genomic variation within virtually anytranscribed element affects its own RNA abundance. Specifically, thisapproach could readily be adopted to study how other transcribedelements contribute to expression levels (e.g. the influence of 5′- and3′ UTRs sequence on RNA stability, etc.). In this context, enhancers aretranscribed at low levels (eRNA), suggesting an approach for studyingenhancer activity, as well.

Additionally, assays such as targeted ChIP-Seq could be performed tocharacterize how libraries of genomic edits affect epigenetic states incoding or non-coding regions. By taking large quantities of DNA fromexpanded populations of edited cells and functionally separating editsbased on biochemical interactions (i.e. transcription factor binding,associated histone modification, nucleosome positioning, etc.),genotype-phenotype associations would be preserved.

Apart from the molecular assays described above, the DBR1 experiment isjust one example of a cell-based assay that can be read out withhigh-throughput sequencing. In addition to essentiality (in haploidcells or diploid cells made functionally haploid through previous genedisruption), gain-of-function (such as drug resistance or growth gain),haploid insufficiency and dominant negative effects could be measuredwith appropriate selection assays. In fact, any well-customized assaythat allows functionally-based separation of cell populations (e.g.,with FACS) is amenable to downstream sequencing of edited populations ofassayed cells as a readout. For instance, reporter cell lines engineeredto express fluorescently tagged genes of interest could be used to assaymultiplex HDR-edited transcription factors or enhancers.

Given the relative ease of targeted nuclease production and mutagenesislibrary cloning, the methods disclosed herein are readily scalable.Exons could be tiled to functionally assess each coding SNV acrossentire genes. Therefore, the methods disclosed herein provide a valuableapproach for determining functional effects of large numbers ofprogrammed genomic mutations in many biological contexts.

REFERENCES

The references, patents and published patent applications listed below,and all references cited in the specification above are herebyincorporated by reference in their entirety, as if fully set forthherein.

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TABLE 1 List of all oligonucleotides used in saturation genome editingexperiments BRCA1 Library Cloning SEQ ID NO Template for random hexamerlibrary BRCA1ex18NNNNNN5_10selPCR (machine-mixing) SEQ ID NO: 1GAGTGTTTTTCATTCTGCAGATGCNNNNNNTGTGTGGATATCCCACACTGAAATATTTTCTAGGAATTGCGGGAGGTo PCR-amplify hexamer library inserts BRCA1ex18_Hexamers_F SEQ ID NO: 2GAGTGTTTTTCATTCTGCAG BRCA1ex18_Hexamers_R SEQ ID NO: 3CCTCCCGCAATTCCTAGAAA To PCR-amplify homologous arms from gDNA with pUC19adaptors pUC_gBRCA1_INF_5′ SEQ ID NO: 4CGGTACCCGGGGATCGAACTCCCGACATCAGGTGA pUC_gBRCA1_INF_3′ SEQ ID NO: 5CGACTCTAGAGGATCAAGGATTCTGTGAGGGAGCA To PCR-linearize pUC19-BRCA1ex18 forrandom hexamer insertion Lin_pUC_BRCA1ex18_5′ SEQ ID NO: 6CTGCAGAATGAAAAACACTC Lin_pUC_BRCA1ex18_3′ SEQ ID NO: 7TTTCTAGGAATTGCGGGAGG BRCA1ex18_3%_mut Template (blue = 97 wt/1/1/1bases; SEQ ID NO: 8ATTCTGCAGATGCTGAGTTTGTGTGTGAACGGACACTGAAATATTTTCTAGGAATTGCGGGAGGAhand-mixing) AAATGGGGAGGAAAATGGGTAGTTAGCTATTTCTGTAAGTATAATAC ToPCR-amplify BRCA1ex18 3% mutation inserts BRCA1ex18_5′1_Amp SEQ ID NO: 9GAGTGTTTTTCATTCTGCAG 5′2_Syn_Amp SEQ ID NO: 10TTCTGCAGATGCTGAGTTTGTCTGCGAGAGAACACTGAAATATTTTC 5′2_Eco_Amp SEQ ID NO:11 TTCTGCAGATGCTGAGTTTGTGTGGATATCCACACTGAAATATTTTC BRCA1ex18_3′1_Amp SEQID NO: 12 GGAGAAATAGTATTATACTTAC 3′2_Syn_Amp SEQ ID NO: 13TTATACTTACAGAAATAGCTTACAACCCACTTACCACCTGCAATTCCTA 3′2_Eco_Amp SEQ ID NO:14 TTATACTTACAGAAATAGCTAAGGATATCTTTTCCTCCCGCAAT To PCR-linearizepUC19_BRCA1ex18 for 3% mutation inserts In-Fusion_Lin_5′1 SEQ ID NO: 15CTGCAGAATGAAAAACACTC In-Fusion_Lin_3′1 SEQ ID NO: 16GTAAGTATAATACTATTTCTCC In-Fusion_Lin_5′2 SEQ ID NO: 17CAAACTCAGCATCTGCAGAA In-Fusion_Lin_3′2 SEQ ID NO: 18AGCTATTTCTGTAAGTATAA pCas9-sgBRCA1x18 cloning sgRNA_BRCA1ex18_F SEQ IDNO: 19 CACCGATGCTGAGTTTGTGTGTGAA sgRNA_BRCA1ex18_R SEQ ID NO: 20AAACTTCACACACAAACTCAGCATC BRCA1 Sample Processing for Sequencing ReverseTranscription BRCA1ex19_RT SEQ ID NO: 21 TTTCTTTCTTTAATAGACTGGGTCABRCA1ex21_RT SEQ ID NO: 22 GTGGGCATGTTGGTGAAG Primer to PCR-amplify fromgDNA external to HDR Library external_BRCA1ex18_F SEQ ID NO: 23CGGCTTTTGTAGCAGTTAAACA gDNA/cDNA hexamer selective PCR primerBRCA1ex18SelPCR_Hex_R 24SEQ ID NO: CCTAGAAAATATTTCAGTGTGGATATC cDNAhexamer PCR primers BRCA1ex16_cDNA1_F SEQ ID NO: 25 GGAGAAGCCAGAATTGACAHexamer sequencing adaptor primers PU1L_BRCA1intron17_F SEQ ID NO: 26CTAAATGGCTGTGAGAGAGCTCAGTGGTGTTTTCAGCCTCTGATT PU1R_BRCA1ex18SelPCR_Hex_RSEQ ID NO: 27 ACTTTATCAATCTCGCTCCAAACCCCTAGAAAATATTTCAGTGTGGATATCPU1L_BRCA1ex16_cDNA2_F SEQ ID NO: 28CTAAATGGCTGTGAGAGAGCTCAGGCTTCAACAGAAAGGGTCA PU1R_BRCA1ex18_3′1_Amp SEQID NO: 29 ACTTTATCAATCTCGCTCCAAACCGGAGAAATAGTATTATACTTAC MiSeq Flowcelland Indexing Primers FC_PU1L SEQ ID NO: 30AATGATACGGCGACCACCGAGATCTACACACGTAGGCCTAAATGGCTGTGAGAGAGCTCAGFC_index_PU1R_142 SEQ ID NO: 31CAAGCAGAAGACGGCATACGAGATAAGCGTTCAGACCGTCGGCACTTTATCAATCTCGCTCCAAACCFC_index_PU1R_143 SEQ ID NO: 32CAAGCAGAAGACGGCATACGAGATCGCAAGCGTGACCGTCGGCACTTTATCAATCTCGCTCCAAACCFC_index_PU1R_144 SEQ ID NO: 33CAAGCAGAAGACGGCATACGAGATGCAGCGCGAGACCGTCGGCACTTTATCAATCTCGCTCCAAACCFC_index_PU1R_145 SEQ ID NO: 34CAAGCAGAAGACGGCATACGAGATCGCGCAGCTGACCGTCGGCACTTTATCAATCTCGCTCCAAACCFC_index_PU1R_146 SEQ ID NO: 35CAAGCAGAAGACGGCATACGAGATTCAAGCGCAGACCGTCGGCACTTTATCAATCTCGCTCCAAACCFC_index_PU1R_147 SEQ ID NO: 36CAAGCAGAAGACGGCATACGAGATCAGTCGCAGGACCGTCGGCACTTTATCAATCTCGCTCCAAACCFC_index_PU1R_148 SEQ ID NO: 37CAAGCAGAAGACGGCATACGAGATGCGTCAGTTGACCGTCGGCACTTTATCAATCTCGCTCCAAACCFC_index_PU1R_149 SEQ ID NO: 38CAAGCAGAAGACGGCATACGAGATAGTCGCGCAGACCGTCGGCACTTTATCAATCTCGCTCCAAACCSelective PCR and seq prep for 3% mut experiments BRCA1ex20_R SEQ ID NO:39 CTTTCTGTCCTGGGATTCTC PU1R_BRCA1ex20 SEQ ID NO: 40ACTTTATCAATCTCGCTCCAAACCCTTTCTGTCCTGGGATTCTC BRCA1ex16_cDNA2_F SEQ IDNO: 41 GCTTCAACAGAAAGGGTCA PU1L_BRCA1ex16_cDNA2_F SEQ ID NO: 42CTAAATGGCTGTGAGAGAGCTCAGGCTTCAACAGAAAGGGTCA PU1L_BRCA1intron17_2 SEQ IDNO: 43 CTAAATGGCTGTGAGAGAGCTCAGCCAGATTGATCTTGGGAGTG PU1R_BRCA1intron18SEQ ID NO: 44 ACTTTATCAATCTCGCTCCAAACCGGTAACTCAGACTCAGCATCBRCA1ex18_sel5Syn_F SEQ ID NO: 45 TGAGTTTGTCTGCGAGAGAPU1L_BRCA1ex18_sel5syn SEQ ID NO: 46CTAAATGGCTGTGAGAGAGCTCAGTGAGTTTGTCTGCGAGAGA BRCA1ex18_sel5Eco_F SEQ IDNO: 47 GCTGAGTTTGTGTGGATATCC PU1L_BRCA1ex18_sel5Eco SEQ ID NO: 48CTAAATGGCTGTGAGAGAGCTCAGGCTGAGTTTGTGTGGATATCC BRCA1ex18_sel3Syn_R SEQ IDNO: 49 TACAACCCACTTACCACCT PU1R_BRCA1ex18_sel3Syn SEQ ID NO: 50ACTTTATCAATCTCGCTCCAAACCTACAACCCACTTACCACCT BRCA1ex18_sel3Eco_R SEQ IDNO: 51 ACTTACAGAAATAGCTAAGGATATC PU1R_BRCA1ex18_sel3Eco SEQ ID NO: 52ACTTTATCAATCTCGCTCCAAACCACTTACAGAAATAGCTAAGGATATC DBR1 HDR LibraryCloning CustomArray DBR1 oligonucleotide pool SEQ ID NO: 53CCAGTTCTCACGCTCTTCATCGGCGGAAACCATGAAGCCTCAATCATTTGCAAGAGTTACCCTATGGTGGGTGGCA(63x codon mutations bold; 225 1bp mutations blue; non-CCAAACATTTATTATTTAGgtatgtgtgatactttgtggatac reference red; intronlower-case) To PCR-amplify HDR library inserts (oligonucleotide pool)Dbr1X2D_AMP_F SEQ ID NO: 54 TCTCACGCTCTTCATCGGCG Dbr1X2D_AMP_R SEQ IDNO: 55 TCCACAAAGTATCACACAT To PCR-amplify homologous arms from Hap1 gDNAwith pUC19 adaptors pUC19_Dbr1_Inf_F SEQ ID NO: 56CGGTACCCGGGGATCGAGGCGGGAAATGTATTCAG pUC19_Dbr1_Inf_R SEQ ID NO: 57CGACTCTAGAGGATCCAGGAAATGCTGCAAGACAA To PCR-linearize pUC19-Dbr1ex2 forlibrary insertion Lin_pUC19-Dbr1X2_5 SEQ ID NO: 58CGCCGATGAAGAGCGTGAGAACTGG Lin_pUC19-Dbr1X2_3 SEQ ID NO: 59ATGTGTGATACTTTGTGGATACTTTTTTTTCCTGGG DBR1 Sample Processing forSequencing To amplify gDNA from outside plasmid homology external_Dbr1_FSEQ ID NO: 60 GCCTGTTTCCCTTAGATCCT Selective PCR from edited gDNADbr1Int2_selAMP_R SEQ ID NO: 61 AGTATCCACAAAGTATCACAC Non-selective PCRfrom edited gDNA Dbr1_Int2_R2 SEQ ID NO: 62 CCTGATAAGCTCTTCCATCC To addadaptors for sequencing PU1L_Dbr1Int1_AMP SEQ ID NO: 63CTAAATGGCTGTGAGAGAGCTCAGGCCTAATTGTGGTAACTGAC PU1R_Dbr1Int2_selAMP_R SEQID NO: 64 ACTTTATCAATCTCGCTCCAAACCAGTATCCACAAAGTATCACACPU1R_Dbr1_Int2_R2 SEQ ID NO: 65ACTTTATCAATCTCGCTCCAAACCCCTGATAAGCTCTTCCATCC pCas9-EGFP-sgDbr1x2 CloningsgRNA_Dbr1X2_F SEQ ID NO: 66 CACCGCAGTTCTCACGCTCTTCATT sgRNA_Dbr1X2_RSEQ ID NO: 67 AAACAATGAAGAGCGTGAGAACTGC Exon sequences in this study SEQID NO: 68 .GAGTGTTTTTCATTCTGCAGATGCTGAGTTTGTGTGTGAACGGACACTGAAATATTTTCTAWT BRCA1ex18 (PAM, protospacer underlined; introns gray)GGAATTGCGGGAGGAAAATGGGTAGTTAGCTATTTCTGTAAGTATAATACTATTTC BRCA1 and DBR1HDR library exons in pUC19 homology donor plasmids HDRL Random HexamerBRCA1ex18 SEQ ID NO: 69...GAGTGTTTTTCATTCTGCAGATGCNNNNNNTGTGTGGATATCCACACTGAAATATTTTCTAGGAATTGCGGGAGGAAAATGGGTAGTTAGCTATTTCTGTAAGTATAATACTATTTC... HDRL 3% mut5′ SYN BRCA1ex18 SEQ ID NO: 70.GAGTGTTTTTCATTCTGCAGATGCTGAGTTTGTCTGCGAGAGAACACTGAAATATTTTCTAGGAATTGCGGGAGGAAAATGGGTAGTTAGCTATTTCTGTAAGTATAATACTATTTC. HDRL 3% mut5′ NONSYN BRCA1ex18 SEQ ID NO: 71...GAGTGTTTTTCATTCTGCAGATGCTGAGTTTGTGTGGATATCCACACTGAAATATTTTCTAGGAATTGCGGGAGGAAAATGGGTAGTTAGCTATTTCTGTAAGTATAATACTATTTC .. HDRL 3% mut3′ NONSYN BRCA1ex18 SEQ ID NO: 72...GAGTGTTTTTCATTCTGCAGATGCTGAGTTTGTGTGTGAACGGACACTGAAATATTTTC(selective PCR sites red; mutated region blue)TAGGAATTGCGGGAGGAAAAGATATCCTTAGCTATTTCTGTAAGTATAATACTATTTC WT DBR1ex2SEQ ID NO: 73...CCAGTTCTCACGCTCTTCATTGGGGGAAACCATGAAGCCTCAAATCATTTGCAAGAGTTACCCTATGGTGGCTGGGTGGCACCAAACATTTATTATTTAGGTATGTGATTGTGTTTGTGGATACDBR1ex2 HDRL SEQ ID NO: 74...CCAGTTCTCACGCTCTTCATCGGCGGAAACCATGAAGCCTCAAATCATTTGCAAGAGTTACCCTATGGTGGCTGGGTGGCACCAAACATTATTATTTAGGTATGTGTGATACTTTGTGGATAC(63x codon substitutions bold, PAM/protospacer mutations green)

TABLE 2 Empirical measurement of impact of introducing 4048 hexamers asgenome edits to BRCA1 exon 18 (+5 to +10) on abundance of exon 18containing transcripts hamming Log2 % in input Ke et al. 2011 nonsensedistance to enrichment Hexamer library ESRseq score hexamer? WT scoreTGAGTT 1.197% NA no 0 0.000 AGAGTT 0.049% NA no 1 −2.087 CGAGTT 0.014%NA no 1 −0.095 GGAGTT 0.040% NA no 1 −0.135 TAAGTT 0.024% −0.493 no 1−0.744 TCAGTT 0.019% −0.311 no 1 −2.260 TGAATT 0.031% NA no 1 0.444TGACTT 0.017% NA no 1 0.436 TGAGAT 0.033% NA no 1 −0.034 TGAGCT 0.019%NA no 1 0.674 TGAGGT 0.034% NA no 1 −0.310 TGAGTA 0.037% NA no 1 0.478TGAGTC 0.016% NA no 1 −0.153 TGAGTG 0.023% NA no 1 −0.227 TGATTT 0.019%NA no 1 −0.051 TGCGTT 0.016% NA no 1 0.309 TGGGTT 0.021% −0.521 no 1−0.685 TGTGTT 0.022% −0.198 no 1 −0.440 TTAGTT 0.017% −0.831 yes 1−4.278 AAAGTT 0.050% NA no 2 −2.917 ACAGTT 0.036% NA no 2 −3.111 AGAATT0.037% NA no 2 −5.548 AGACTT 0.032% NA no 2 −3.599 AGAGAT 0.053%  0.367no 2 −2.453 AGAGCT 0.033% NA no 2 −0.866 AGAGGT 0.054% NA no 2 −2.970AGAGTA 0.062% NA no 2 −4.019 AGAGTC 0.039%  0.300 no 2 −3.721 AGAGTG0.059% NA no 2 −3.279 AGATTT 0.032% NA no 2 −3.706 AGCGTT 0.028% NA no 2−0.376 AGGGTT 0.051% −0.470 no 2 −5.913 AGTGTT 0.035% NA no 2 −0.708ATAGTT 0.030% −0.554 yes 2 −5.399 CAAGTT 0.020% NA no 2 −1.781 CGAATT0.023% NA no 2 0.094 CGACTT 0.010% NA no 2 −0.889 CGAGAT 0.023%  0.348no 2 0.637 CGAGCT 0.015% NA no 2 1.281 CGAGGT 0.019% NA no 2 −0.099CGAGTA 0.022% NA no 2 −1.055 CGAGTC 0.011%  0.399 no 2 −1.001 CGAGTG0.018%  0.165 no 2 −0.742 CGATTT 0.008% NA no 2 −1.125 CGCGTT 0.008% 0.316 no 2 0.643 CGGGTT 0.017% NA no 2 0.523 CGTGTT 0.008% NA no 2−0.268 CTAGTT 0.007% −0.555 yes 2 −3.727 GAAGTT 0.040%  0.468 no 2−1.915 GCAGTT 0.027% NA no 2 −1.427 GGAATT 0.044%  0.242 no 2 −1.710GGACTT 0.028%  0.338 no 2 0.237 GGAGAT 0.058%  0.336 no 2 −0.559 GGAGCT0.034% NA no 2 −0.362 GGAGGT 0.043% NA no 2 −0.966 GGAGTA 0.053% NA no 2−0.989 GGAGTC 0.031%  0.516 no 2 1.196 GGAGTG 0.051% NA no 2 0.448GGATTT 0.037% NA no 2 0.511 GGCGTT 0.014%  0.278 no 2 0.622 GGGGTT0.038% −0.543 no 2 −1.880 GGTGTT 0.023% NA no 2 0.407 GTAGTT 0.020%−0.658 yes 2 −5.724 TAAATT 0.026% −0.632 no 2 −3.111 TAACTT 0.021%−0.457 no 2 −3.257 TAAGAT 0.035% NA no 2 −4.842 TAAGCT 0.023% −0.368 no2 −3.123 TAAGGT 0.041% −0.468 no 2 −5.926 TAAGTA 0.037% −0.667 no 2−5.980 TAAGTC 0.018% NA no 2 −4.899 TAAGTG 0.029% −0.461 no 2 −2.670TAATTT 0.019% −0.389 no 2 −2.975 TACGTT 0.016% NA no 2 −0.949 TAGGTT0.020% −0.796 no 2 −4.864 TATGTT 0.022% −0.301 no 2 0.809 TCAATT 0.018%NA no 2 −1.685 TCACTT 0.020% NA no 2 −2.880 TCAGAT 0.030% NA no 2 −2.559TCAGCT 0.018% NA no 2 −1.810 TCAGGT 0.034% −0.438 no 2 −3.941 TCAGTA0.027% −0.407 no 2 −4.288 TCAGTC 0.019% NA no 2 −3.280 TCAGTG 0.019%−0.267 no 2 −1.379 TCATTT 0.021% NA no 2 −1.268 TCCGTT 0.010% NA no 2−1.495 TCGGTT 0.009% NA no 2 0.288 TCTGTT 0.009% NA no 2 −3.347 TGAAAT0.044%  0.190 no 2 0.723 TGAACT 0.025%  0.339 no 2 0.102 TGAAGT 0.040% 0.384 no 2 0.269 TGAATA 0.039% NA no 2 −0.574 TGAATC 0.023%  0.426 no 20.250 TGAATG 0.033%  0.131 no 2 −0.509 TGACAT 0.028%  0.198 no 2 −0.058TGACCT 0.016%  0.459 no 2 0.587 TGACGT 0.020%  0.482 no 2 −0.401 TGACTA0.020% NA no 2 −0.011 TGACTC 0.014%  0.281 no 2 0.808 TGACTG 0.025% 0.319 no 2 0.017 TGAGAA 0.042%  0.338 no 2 −0.485 TGAGAC 0.023%  0.379no 2 0.426 TGAGAG 0.039% NA no 2 0.032 TGAGCA 0.032% NA no 2 0.825TGAGCC 0.013% NA no 2 −0.385 TGAGCG 0.028%  0.298 no 2 −0.504 TGAGGA0.045%  0.459 no 2 −0.578 TGAGGC 0.026% NA no 2 −0.340 TGAGGG 0.036%−0.255 no 2 −0.259 TGATAT 0.020% NA no 2 0.376 TGATCT 0.014%  0.250 no 2−0.824 TGATGT 0.023%  0.187 no 2 −0.087 TGATTA 0.025% −0.400 no 2 −1.266TGATTC 0.015% NA no 2 0.431 TGATTG 0.023% NA no 2 −0.434 TGCATT 0.015%−0.326 no 2 0.675 TGCCTT 0.012% −0.306 no 2 −0.259 TGCGAT 0.021% NA no 2−0.172 TGCGCT 0.014% NA no 2 0.218 TGCGGT 0.025% NA no 2 0.378 TGCGTA0.027% −0.382 no 2 −0.825 TGCGTC 0.013%  0.277 no 2 0.398 TGCGTG 0.018%NA no 2 −0.198 TGCTTT 0.016% −0.394 no 2 −0.653 TGGATT 0.017%  0.323 no2 1.166 TGGCTT 0.019% NA no 2 0.058 TGGGAT 0.029% NA no 2 −0.353 TGGGCT0.017% −0.259 no 2 0.128 TGGGGT 0.023% −0.511 no 2 −0.953 TGGGTA 0.039%−0.617 no 2 −0.059 TGGGTC 0.013% −0.279 no 2 0.302 TGGGTG 0.024% −0.379no 2 0.271 TGGTTT 0.020% −0.337 no 2 0.517 TGTATT 0.019% −0.319 no 20.378 TGTCTT 0.017% NA no 2 −0.008 TGTGAT 0.027%  0.111 no 2 0.512TGTGCT 0.018% −0.251 no 2 0.576 TGTGGT 0.020% NA no 2 0.449 TGTGTA0.021% −0.320 no 2 0.571 TGTGTC 0.016% −0.091 no 2 −0.114 TGTGTG 0.018%−0.073 no 2 −0.106 TGTTTT 0.017% −0.323 no 2 −1.622 TTAATT 0.021% −0.507yes 2 −5.963 TTACTT 0.010% NA no 2 −1.858 TTAGAT 0.029% −0.578 yes 2−6.001 TTAGCT 0.011% −0.539 yes 2 −6.151 TTAGGT 0.020% −0.783 yes 2−5.014 TTAGTA 0.022% −0.852 yes 2 −7.070 TTAGTC 0.013% −0.539 yes 2−3.757 TTAGTG 0.018% −0.572 yes 2 −4.719 TTATTT 0.018% −0.387 no 2−4.650 TTCGTT 0.010%  0.263 no 2 0.414 TTGGTT 0.016% −0.279 no 2 −2.771TTTGTT 0.014% −0.219 no 2 −4.474 AAAATT 0.041% −0.420 no 3 −3.370 AAACTT0.036% NA no 3 −3.803 AAAGAT 0.060% NA no 3 −2.175 AAAGCT 0.045% NA no 3−1.456 AAAGGT 0.067% NA no 3 −3.660 AAAGTA 0.068% NA no 3 −3.718 AAAGTC0.045% NA no 3 −3.758 AAAGTG 0.066% NA no 3 −0.446 AAATTT 0.032% −0.321no 3 −5.043 AACGTT 0.027%  0.344 no 3 −1.254 AAGGTT 0.039% NA no 3−3.706 AATGTT 0.032% NA no 3 −3.322 ACAATT 0.039% NA no 3 −2.812 ACACTT0.024% NA no 3 −0.816 ACAGAT 0.043%  0.254 no 3 −1.121 ACAGCT 0.032% NAno 3 −1.664 ACAGGT 0.047% −0.315 no 3 −3.492 ACAGTA 0.045% NA no 3−3.203 ACAGTC 0.029% NA no 3 −2.148 ACAGTG 0.044% −0.161 no 3 −1.459ACATTT 0.033% NA no 3 −3.087 ACCGTT 0.017% NA no 3 −0.727 ACGGTT 0.033%NA no 3 −1.170 ACTGTT 0.023% NA no 3 −2.396 AGAAAT 0.069% NA no 3 −5.660AGAACT 0.037%  0.370 no 3 −6.371 AGAAGT 0.057%  0.423 no 3 −5.238 AGAATA0.052% NA no 3 −6.123 AGAATC 0.036%  0.368 no 3 −7.624 AGAATG 0.032% 0.157 no 3 −3.970 AGACAT 0.048% NA no 3 −2.164 AGACCT 0.024%  0.540 no3 −0.409 AGACGT 0.032%  0.542 no 3 −0.938 AGACTA 0.037% NA no 3 −3.628AGACTC 0.030% NA no 3 −2.106 AGACTG 0.027%  0.372 no 3 −0.327 AGAGAA0.078%  0.392 no 3 −3.001 AGAGAC 0.048%  0.535 no 3 −1.922 AGAGAG 0.062%NA no 3 −0.588 AGAGCA 0.049% NA no 3 −2.611 AGAGCC 0.034% NA no 3 −1.864AGAGCG 0.046% NA no 3 −0.458 AGAGGA 0.072%  0.526 no 3 −2.083 AGAGGC0.053% NA no 3 −2.144 AGAGGG 0.067% −0.155 no 3 −1.469 AGATAT 0.044% NAno 3 −3.245 AGATCT 0.026%  0.293 no 3 −4.228 AGATGT 0.032% NA no 3−2.907 AGATTA 0.048% NA no 3 −3.769 AGATTC 0.034% NA no 3 −3.977 AGATTG0.039% NA no 3 −1.023 AGCATT 0.030% NA no 3 −0.977 AGCCTT 0.020% −0.300no 3 −0.676 AGCGAT 0.034% NA no 3 0.558 AGCGGT 0.034% NA no 3 −0.746AGCGTA 0.039% NA no 3 0.056 AGCGTC 0.024%  0.515 no 3 0.682 AGCGTG0.031% NA no 3 −0.212 AGCTTT 0.016% −0.353 no 3 0.785 AGGATT 0.044% NAno 3 −4.617 AGGCTT 0.027% NA no 3 −3.483 AGGGAT 0.059% NA no 3 −4.510AGGGCT 0.038% NA no 3 −4.903 AGGGGT 0.059% −0.340 no 3 −5.948 AGGGTA0.063% −0.535 no 3 −8.531 AGGGTC 0.040% NA no 3 −8.002 AGGGTG 0.054%−0.480 no 3 −1.698 AGGTTT 0.033% −0.434 no 3 −4.722 AGTATT 0.038% −0.387no 3 −1.655 AGTCTT 0.024% NA no 3 −1.285 AGTGAT 0.043% NA no 3 −0.797AGTGCT 0.028% −0.116 no 3 −1.139 AGTGGT 0.037% NA no 3 −0.459 AGTGTA0.049% −0.354 no 3 −1.193 AGTGTC 0.030% NA no 3 −1.323 AGTGTG 0.039%−0.255 no 3 −0.577 AGTTTT 0.022% −0.106 no 3 −1.689 ATAATT 0.042% −0.326yes 3 −4.629 ATACTT 0.029% −0.253 no 3 −3.405 ATAGAT 0.041% NA yes 3−7.247 ATAGCT 0.021% −0.266 yes 3 −3.911 ATAGGT 0.031% −0.528 yes 3−6.841 ATAGTA 0.038% −0.504 yes 3 −8.063 ATAGTC 0.023% NA yes 3 −8.443ATAGTG 0.041% −0.337 yes 3 −4.360 ATATTT 0.031% −0.534 no 3 −3.525ATCGTT 0.022% NA no 3 0.820 ATGGTT 0.032% −0.289 no 3 −5.190 ATTGTT0.030% NA no 3 −3.539 CAAATT 0.021% −0.223 no 3 −1.563 CAACTT 0.017% NAno 3 0.004 CAAGAT 0.035%  0.638 no 3 0.017 CAAGCT 0.018%  0.212 no 3−2.428 CAAGGT 0.026% NA no 3 −2.327 CAAGTA 0.028% NA no 3 −2.177 CAAGTC0.016%  0.334 no 3 −1.227 CAAGTG 0.025% NA no 3 −0.641 CAATTT 0.014% NAno 3 −3.535 CACGTT 0.015% NA no 3 −1.326 CAGGTT 0.023% −0.433 no 3−3.256 CATGTT 0.016% NA no 3 −1.058 CCAATT 0.010% −0.476 no 3 −2.859CCACTT 0.013% −0.386 no 3 −2.052 CCAGAT 0.024% NA no 3 0.033 CCAGCT0.016% −0.365 no 3 0.244 CCAGGT 0.017% −0.325 no 3 −0.936 CCAGTA 0.018%−0.671 no 3 −1.440 CCAGTC 0.012% −0.219 no 3 −0.429 CCAGTG 0.015% −0.143no 3 −1.218 CCATTT 0.009% −0.590 no 3 −0.899 CCCGTT 0.007% NA no 3−0.463 CCGGTT 0.011% NA no 3 0.340 CCTGTT 0.009% NA no 3 1.394 CGAAAT0.026% NA no 3 −0.612 CGAACT 0.016%  0.321 no 3 −0.873 CGAAGT 0.020% 0.353 no 3 0.893 CGAATA 0.027% NA no 3 −0.691 CGAATC 0.015%  0.352 no 30.276 CGAATG 0.027%  0.207 no 3 −1.068 CGACAT 0.020%  0.286 no 3 −0.265CGACCT 0.009%  0.288 no 3 −0.156 CGACGT 0.017%  0.644 no 3 1.045 CGACTA0.012% NA no 3 −1.372 CGACTC 0.010% NA no 3 2.608 CGACTG 0.014%  0.515no 3 −0.431 CGAGAA 0.025% NA no 3 1.080 CGAGAC 0.013% NA no 3 1.099CGAGAG 0.020%  0.390 no 3 −1.104 CGAGCA 0.019% NA no 3 0.394 CGAGCC0.009%  0.281 no 3 −0.259 CGAGCG 0.015%  0.531 no 3 −0.071 CGAGGA 0.021% 0.471 no 3 0.149 CGAGGC 0.016%  0.427 no 3 0.046 CGAGGG 0.026%  0.233no 3 0.945 CGATAT 0.016% NA no 3 −1.021 CGATCT 0.008% NA no 3 −1.982CGATGT 0.015% NA no 3 0.447 CGATTA 0.013% −0.393 no 3 0.253 CGATTC0.010% NA no 3 3.144 CGATTG 0.013%  0.149 no 3 1.897 CGCATT 0.012% NA no3 −0.884 CGCCTT 0.007% NA no 3 0.871 CGCGAT 0.015%  0.491 no 3 −0.672CGCGCT 0.006%  0.393 no 3 3.124 CGCGGT 0.011%  0.296 no 3 0.299 CGCGTA0.014% NA no 3 −1.456 CGCGTC 0.009%  0.675 no 3 1.729 CGCGTG 0.008% 0.357 no 3 1.836 CGCTTT 0.009% NA no 3 0.506 CGGATT 0.016%  0.372 no 3−0.897 CGGCTT 0.007% NA no 3 0.312 CGGGAT 0.026%  0.420 no 3 0.223CGGGCT 0.015% NA no 3 0.553 CGGGGT 0.018% NA no 3 −1.640 CGGGTA 0.025%NA no 3 0.462 CGGGTC 0.014% NA no 3 0.464 CGGGTG 0.013% NA no 3 −0.247CGGTTT 0.014% NA no 3 −1.467 CGTATT 0.009% NA no 3 1.250 CGTCTT 0.010%NA no 3 −2.684 CGTGAT 0.015%  0.311 no 3 −1.066 CGTGGT 0.009%  0.292 no3 −1.389 CGTGTC 0.010%  0.418 no 3 −0.261 CGTGTG 0.013% NA no 3 −0.237CGTTTT 0.007% NA no 3 1.457 CTAATT 0.011% −0.682 yes 3 −5.037 CTACTT0.006% NA no 3 −0.406 CTAGCT 0.008% −0.441 yes 3 −8.166 CTAGGT 0.010%−0.665 yes 3 −2.775 CTAGTA 0.011% −0.925 yes 3 −5.226 CTAGTC 0.008%−0.378 yes 3 −5.593 CTAGTG 0.010% −0.387 yes 3 −6.779 CTCGTT 0.005% NAno 3 0.338 CTGGTT 0.010% NA no 3 −0.543 CTTGTT 0.011% −0.302 no 3 −2.109GAAATT 0.041% NA no 3 −2.356 GAACTT 0.029%  0.297 no 3 −2.602 GAAGAT0.051%  0.992 no 3 0.259 GAAGCT 0.034%  0.476 no 3 −0.995 GAAGGT 0.044%NA no 3 −0.347 GAAGTA 0.057% NA no 3 −1.588 GAAGTC 0.034%  0.614 no 3−0.335 GAAGTG 0.044%  0.247 no 3 −0.013 GAATTT 0.036% NA no 3 −2.861GACGTT 0.021%  0.592 no 3 0.041 GAGGTT 0.032% −0.250 no 3 −3.208 GATGTT0.025%  0.289 no 3 −1.072 GCAATT 0.020% NA no 3 −2.914 GCACTT 0.020%−0.392 no 3 −0.899 GCAGAT 0.035% NA no 3 −3.309 GCAGCT 0.023% −0.113 no3 −1.761 GCAGGT 0.032% −0.475 no 3 −3.457 GCAGTA 0.036% −0.297 no 3−0.890 GCAGTC 0.019% NA no 3 −2.739 GCAGTG 0.039% NA no 3 −1.098 GCATTT0.017% −0.179 no 3 −0.876 GCCGTT 0.019% NA no 3 −0.043 GCGGTT 0.019% NAno 3 −2.216 GCTGTT 0.017% NA no 3 0.130 GGAAAT 0.066%  0.176 no 3 −0.475GGAACT 0.046%  0.428 no 3 0.155 GGAAGT 0.057%  0.249 no 3 0.112 GGAATA0.066% NA no 3 −1.106 GGAATC 0.043%  0.485 no 3 0.551 GGAATG 0.062% 0.208 no 3 −1.925 GGACAT 0.042%  0.452 no 3 0.202 GGACCT 0.029%  0.675no 3 −0.141 GGACGT 0.034%  0.642 no 3 0.326 GGACTA 0.040%  0.212 no 30.117 GGACTC 0.021%  0.357 no 3 0.563 GGACTG 0.038%  0.479 no 3 −0.061GGAGAA 0.075%  0.346 no 3 0.683 GGAGAC 0.041%  0.555 no 3 0.194 GGAGAG0.057% NA no 3 −0.267 GGAGCA 0.056%  0.193 no 3 −0.902 GGAGCC 0.026% 0.507 no 3 0.546 GGAGCG 0.039%  0.339 no 3 0.798 GGAGGA 0.060%  0.409no 3 0.328 GGAGGC 0.033%  0.361 no 3 0.855 GGAGGG 0.058% −0.143 no 3−0.684 GGATAT 0.041% NA no 3 −0.148 GGATCT 0.032% NA no 3 0.188 GGATGT0.040%  0.229 no 3 −0.189 GGATTA 0.048% NA no 3 −0.693 GGATTC 0.030% 0.464 no 3 0.476 GGATTG 0.036%  0.244 no 3 0.652 GGCATT 0.022% −0.082no 3 −0.580 GGCCTT 0.013% NA no 3 −2.576 GGCGAT 0.023%  0.316 no 3−0.263 GGCGCT 0.014%  0.188 no 3 1.147 GGCGGT 0.025% NA no 3 1.035GGCGTA 0.027% NA no 3 −0.527 GGCGTC 0.019%  0.613 no 3 0.207 GGCGTG0.018%  0.188 no 3 −0.668 GGCTTT 0.013% −0.234 no 3 −1.419 GGGATT 0.033%NA no 3 0.234 GGGCTT 0.021% −0.350 no 3 −0.716 GGGGAT 0.049% −0.238 no 3−0.226 GGGGCT 0.032% −0.400 no 3 −0.763 GGGGGT 0.040% −0.654 no 3 −1.990GGGGTA 0.050% −0.594 no 3 −0.603 GGGGTC 0.027% −0.349 no 3 −1.000 GGGGTG0.038% −0.457 no 3 0.388 GGGTTT 0.028% −0.581 no 3 −1.389 GGTATT 0.025%−0.474 no 3 −0.435 GGTCTT 0.016% −0.179 no 3 −0.127 GGTGAT 0.035% NA no3 0.495 GGTGCT 0.019% −0.189 no 3 1.239 GGTGGT 0.026% −0.454 no 3 0.208GGTGTA 0.035% −0.244 no 3 0.050 GGTGTC 0.021% NA no 3 0.167 GGTGTG0.031% −0.217 no 3 −0.378 GGTTTT 0.022% −0.371 no 3 0.528 GTAATT 0.024%−0.589 yes 3 −2.628 GTACTT 0.020% −0.338 no 3 −3.345 GTAGAT 0.042%−0.455 yes 3 −6.967 GTAGCT 0.021% −0.471 yes 3 −6.518 GTAGGT 0.033%−0.709 yes 3 −6.858 GTAGTA 0.034% −0.666 yes 3 −5.616 GTAGTC 0.019%−0.348 yes 3 −6.261 GTAGTG 0.026% −0.390 yes 3 −3.622 GTATTT 0.026%−0.477 no 3 −5.037 GTCGTT 0.017% NA no 3 −0.515 GTGGTT 0.020% −0.158 no3 −1.517 GTTGTT 0.012% NA no 3 −2.903 TAAAAT 0.038% −0.616 no 3 −5.006TAAACT 0.028% −0.351 no 3 −3.662 TAAAGT 0.043% −0.299 no 3 −4.139 TAAATA0.030% −0.601 no 3 −3.979 TAAATC 0.022% −0.298 no 3 −7.739 TAAATG 0.031%−0.486 no 3 −1.724 TAACAT 0.035% NA no 3 −5.569 TAACCT 0.016% NA no 3−4.175 TAACGT 0.027% NA no 3 −2.501 TAACTA 0.025% −0.440 no 3 −4.034TAACTC 0.017% NA no 3 −3.670 TAACTG 0.022% −0.235 no 3 −0.752 TAAGAA0.055% NA no 3 −3.674 TAAGAC 0.028% NA no 3 −4.744 TAAGAG 0.038% −0.362no 3 −1.026 TAAGCA 0.037% −0.402 no 3 −5.206 TAAGCC 0.018% −0.286 no 3−4.348 TAAGCG 0.030% NA no 3 −1.758 TAAGGA 0.036% NA no 3 −5.836 TAAGGC0.023% −0.372 no 3 −5.147 TAAGGG 0.045% −0.466 no 3 −4.923 TAATAT 0.022%−0.539 no 3 −4.854 TAATCT 0.017% NA no 3 −6.017 TAATGT 0.022% −0.340 no3 −5.765 TAATTA 0.031% −0.642 no 3 −5.341 TAATTC 0.020% −0.483 no 3−7.396 TAATTG 0.023% −0.563 no 3 −1.442 TACATT 0.017% −0.302 no 3 −2.043TACCTT 0.007% NA no 3 −2.904 TACGAT 0.018% NA no 3 0.187 TACGCT 0.011%NA no 3 −1.509 TACGGT 0.018% NA no 3 −1.481 TACGTA 0.020% NA no 3 −0.495TACGTC 0.013%  0.501 no 3 3.451 TACGTG 0.014% NA no 3 0.538 TACTTT0.010% −0.357 no 3 −3.068 TAGATT 0.019% −0.550 no 3 −6.172 TAGCTT 0.013%−0.691 no 3 −6.108 TAGGAT 0.025% −0.343 no 3 −4.815 TAGGCT 0.014% −0.609no 3 −8.651 TAGGGT 0.028% −0.822 no 3 −8.320 TAGGTA 0.031% −0.997 no 3−8.642 TAGGTC 0.010% −0.723 no 3 −7.192 TAGGTG 0.028% −0.594 no 3 −4.297TAGTTT 0.015% −0.678 no 3 −6.430 TATATT 0.029% −0.716 no 3 −5.131 TATCTT0.011% −0.287 no 3 −6.037 TATGAT 0.028% NA no 3 −3.092 TATGCT 0.015%−0.210 no 3 −3.754 TATGGT 0.025% −0.271 no 3 −3.190 TATGTA 0.028% −0.546no 3 −3.796 TATGTC 0.024% NA no 3 −4.029 TATGTG 0.025% −0.253 no 3−2.263 TATTTT 0.019% −0.564 no 3 −6.436 TCAAAT 0.029% NA no 3 −2.787TCAACT 0.016%  0.275 no 3 −0.972 TCAAGT 0.031% NA no 3 −0.725 TCAATA0.027% NA no 3 −1.793 TCAATC 0.018% NA no 3 −4.515 TCAATG 0.023% NA no 3−0.014 TCACAT 0.021% NA no 3 −2.039 TCACCT 0.012%  0.270 no 3 −1.313TCACGT 0.014% NA no 3 −0.998 TCACTA 0.018% NA no 3 −0.889 TCACTC 0.014%NA no 3 −1.772 TCACTG 0.016% NA no 3 −0.806 TCAGAA 0.047% NA no 3 −4.515TCAGAC 0.021% NA no 3 −2.038 TCAGAG 0.035% NA no 3 −0.865 TCAGCA 0.025%NA no 3 −3.365 TCAGCC 0.012% −0.241 no 3 −2.827 TCAGCG 0.022%  0.343 no3 0.375 TCAGGA 0.034% NA no 3 −0.819 TCAGGC 0.016% NA no 3 −3.842 TCAGGG0.033% −0.370 no 3 −3.648 TCATAT 0.017% NA no 3 −2.724 TCATCT 0.014% 0.329 no 3 −0.379 TCATGT 0.021% NA no 3 −1.760 TCATTA 0.025% NA no 3−4.234 TCATTC 0.017% NA no 3 −2.387 TCATTG 0.016% NA no 3 −0.997 TCCATT0.009% −0.265 no 3 −2.492 TCCCTT 0.009% −0.278 no 3 −0.816 TCCGAT 0.011%NA no 3 −1.785 TCCGCT 0.010% NA no 3 −0.905 TCCGGT 0.010% NA no 3 0.209TCCGTA 0.012% NA no 3 0.018 TCCGTC 0.008%  0.514 no 3 −0.799 TCCGTG0.008%  0.274 no 3 0.624 TCGATT 0.014% NA no 3 −2.198 TCGCTT 0.010% NAno 3 −5.211 TCGGAT 0.022%  0.495 no 3 −0.641 TCGGCT 0.016%  0.287 no 3−1.098 TCGGGT 0.019% NA no 3 −0.018 TCGGTA 0.020% NA no 3 −1.295 TCGGTC0.012%  0.427 no 3 −0.464 TCGGTG 0.020% NA no 3 −0.376 TCGTTT 0.010% NAno 3 −0.219 TCTCTT 0.010% NA no 3 −3.415 TCTGAT 0.015% NA no 3 −1.266TCTGCT 0.011%  0.232 no 3 −1.122 TCTGGT 0.014% NA no 3 −2.332 TCTGTA0.016% NA no 3 −1.150 TCTGTC 0.015% NA no 3 −3.655 TCTGTG 0.015% NA no 3−1.585 TCTTTT 0.015% −0.284 no 3 −7.775 TGAAAA 0.045% NA no 3 −0.600TGAAAC 0.028%  0.263 no 3 −0.135 TGAAAG 0.049% NA no 3 −0.400 TGAACA0.036%  0.267 no 3 −0.244 TGAACC 0.022%  0.252 no 3 −1.184 TGAACG 0.036% 0.515 no 3 0.040 TGAAGA 0.045%  0.943 no 3 0.059 TGAAGC 0.029%  0.521no 3 −0.184 TGAAGG 0.050%  0.166 no 3 −0.633 TGACAA 0.037%  0.229 no 3−0.700 TGACAC 0.018% NA no 3 −0.663 TGACAG 0.035% NA no 3 −0.803 TGACCA0.023%  0.293 no 3 −1.279 TGACCC 0.013% NA no 3 0.342 TGACCG 0.018% 0.547 no 3 1.260 TGACGA 0.025%  0.717 no 3 −0.063 TGACGC 0.015%  0.539no 3 −0.065 TGACGG 0.032%  0.511 no 3 −0.330 TGATAA 0.034% −0.373 no 3−1.068 TGATAC 0.021% NA no 3 0.083 TGATAG 0.039% −0.446 no 3 −0.368TGATCA 0.024% NA no 3 −0.254 TGATCC 0.010%  0.172 no 3 −0.561 TGATCG0.021%  0.536 no 3 −0.187 TGATGA 0.024%  0.451 no 3 0.825 TGATGC 0.019% 0.140 no 3 −0.150 TGATGG 0.033%  0.215 no 3 −0.654 TGCAAT 0.026% −0.466no 3 −0.898 TGCACT 0.016% −0.272 no 3 0.361 TGCAGT 0.020% −0.227 no 3−1.736 TGCATA 0.022% −0.622 no 3 0.019 TGCATC 0.016% NA no 3 −0.201TGCATG 0.019% NA no 3 1.544 TGCCAT 0.018% −0.287 no 3 0.349 TGCCCT0.010% −0.267 no 3 −0.272 TGCCGT 0.013% NA no 3 −1.273 TGCCTA 0.011%−0.641 no 3 −0.768 TGCCTC 0.012% NA no 3 −0.002 TGCCTG 0.010%  0.154 no3 0.076 TGCGAA 0.031% NA no 3 −0.027 TGCGAC 0.021%  0.357 no 3 0.251TGCGAG 0.022% NA no 3 −0.411 TGCGCA 0.018% NA no 3 −0.683 TGCGCC 0.015% 0.309 no 3 0.544 TGCGCG 0.017%  0.311 no 3 0.159 TGCGGA 0.029%  0.458no 3 0.733 TGCGGC 0.020% NA no 3 −0.896 TGCGGG 0.024%  0.298 no 3 0.135TGCTAT 0.015% −0.323 no 3 0.629 TGCTCT 0.014% −0.181 no 3 −0.038 TGCTGT0.018% NA no 3 0.114 TGCTTA 0.019% −0.584 no 3 −0.135 TGCTTC 0.010% NAno 3 0.307 TGCTTG 0.013% −0.181 no 3 −1.193 TGGAAT 0.039%  0.326 no 30.467 TGGACT 0.017%  0.449 no 3 1.333 TGGAGT 0.030%  0.275 no 3 −0.605TGGATA 0.034%  0.123 no 3 −0.884 TGGATC 0.014%  0.359 no 3 1.283 TGGATG0.034%  0.414 no 3 0.515 TGGCAT 0.029% NA no 3 0.327 TGGCCT 0.013% NA no3 −0.865 TGGCGT 0.018%  0.321 no 3 0.781 TGGCTA 0.019% −0.156 no 3−0.691 TGGCTC 0.009% NA no 3 −1.112 TGGCTG 0.022%  0.169 no 3 −0.952TGGGAA 0.044% NA no 3 −0.213 TGGGAC 0.025%  0.286 no 3 −0.590 TGGGAG0.032%  0.077 no 3 −0.855 TGGGCA 0.029% −0.105 no 3 0.600 TGGGCC 0.014%NA no 3 −0.785 TGGGCG 0.018% NA no 3 0.933 TGGGGA 0.037% −0.113 no 30.433 TGGGGC 0.021% −0.149 no 3 −0.473 TGGGGG 0.032% −0.413 no 3 −0.787TGGTAT 0.023% −0.363 no 3 −0.380 TGGTCT 0.016% NA no 3 −0.378 TGGTGT0.023% NA no 3 −0.162 TGGTTA 0.021% −0.457 no 3 −0.466 TGGTTC 0.013% NAno 3 0.216 TGGTTG 0.022% −0.211 no 3 −1.223 TGTAAT 0.029% −0.389 no 3−0.246 TGTACT 0.014% NA no 3 −1.112 TGTAGT 0.024% −0.492 no 3 0.273TGTATA 0.034% −0.526 no 3 −0.677 TGTATC 0.018% NA no 3 0.045 TGTATG0.030% −0.152 no 3 0.022 TGTCAT 0.015% NA no 3 0.044 TGTCCT 0.011% NA no3 1.450 TGTCGT 0.013%  0.280 no 3 −0.371 TGTCTA 0.012% −0.259 no 3−0.468 TGTCTC 0.015% NA no 3 0.228 TGTCTG 0.017% NA no 3 −0.289 TGTGAA0.036%  0.381 no 3 −0.270 TGTGAC 0.019%  0.329 no 3 −0.279 TGTGAG 0.028% 0.171 no 3 0.107 TGTGCA 0.021% −0.247 no 3 −0.470 TGTGCG 0.019% −0.081no 3 −0.277 TGTGGA 0.021%  0.595 no 3 −1.476 TGTGGC 0.019%  0.063 no 3−0.805 TGTGGG 0.030% −0.060 no 3 −0.614 TGTTAT 0.023% −0.263 no 3 −0.909TGTTCT 0.011% NA no 3 0.257 TGTTGT 0.018% NA no 3 0.259 TGTTTA 0.021%−0.532 no 3 0.716 TGTTTC 0.012% NA no 3 −0.515 TGTTTG 0.015% −0.161 no 3−0.273 TTAAAT 0.028% −0.558 yes 3 −5.460 TTAACT 0.025% −0.216 yes 3−3.918 TTAAGT 0.028% −0.496 yes 3 −6.742 TTAATA 0.023% −0.424 yes 3−6.554 TTAATC 0.025% NA yes 3 −8.686 TTAATG 0.029% −0.404 yes 3 −4.133TTACAT 0.020% NA no 3 −3.758 TTACCT 0.010%  0.221 no 3 −1.043 TTACGT0.010% NA no 3 −0.727 TTACTA 0.013% NA no 3 −2.319 TTACTC 0.016% NA no 3−5.081 TTACTG 0.017% NA no 3 −0.218 TTAGAA 0.034% −0.513 yes 3 −8.530TTAGAC 0.016% −0.392 yes 3 −6.524 TTAGAG 0.029% −0.545 yes 3 −4.639TTAGCA 0.023% −0.523 yes 3 −7.346 TTAGCC 0.009% −0.575 yes 3 −6.467TTAGCG 0.021% −0.326 yes 3 −5.679 TTAGGA 0.025% −0.627 yes 3 −5.762TTAGGC 0.011% −0.712 yes 3 −5.624 TTAGGG 0.027% −0.827 yes 3 −7.215TTATAT 0.021% −0.461 no 3 −2.689 TTATCT 0.009% NA no 3 −3.800 TTATGT0.018% −0.272 no 3 −4.521 TTATTA 0.022% −0.478 no 3 −4.891 TTATTC 0.016%NA no 3 −5.148 TTATTG 0.023% −0.343 no 3 −0.759 TTCATT 0.014% NA no 3−1.816 TTCGAT 0.016%  0.344 no 3 0.678 TTCGCT 0.011%  0.308 no 3 −1.573TTCGGT 0.014% NA no 3 0.331 TTCGTA 0.013% NA no 3 −1.039 TTCGTC 0.010% 0.789 no 3 −0.765 TTCGTG 0.012%  0.334 no 3 −0.550 TTCTTT 0.010% −0.207no 3 −3.591 TTGATT 0.017% NA yes 3 −2.576 TTGCTT 0.009% NA no 3 −2.608TTGGAT 0.027%  0.261 no 3 −0.211 TTGGCT 0.015% NA no 3 −0.851 TTGGGT0.025% −0.453 no 3 −5.418 TTGGTA 0.023% −0.369 no 3 −3.830 TTGGTC 0.011%NA no 3 −2.246 TTGGTG 0.015% −0.173 no 3 0.241 TTGTTT 0.016% −0.196 no 3−2.805 TTTATT 0.013% −0.491 no 3 −4.281 TTTCTT 0.011% −0.214 no 3 −6.475TTTGAT 0.015% NA no 3 −3.027 TTTGCT 0.011% −0.219 no 3 −1.789 TTTGGT0.021% −0.323 no 3 −4.850 TTTGTA 0.018% −0.291 no 3 −3.348 TTTGTC 0.015%NA no 3 −2.165 TTTGTG 0.019% −0.222 no 3 −0.369 TTTTTT 0.011% −0.381 no3 −4.402 AAAAAT 0.088% −0.343 no 4 −3.516 AAAACT 0.051% NA no 4 −2.594AAAAGT 0.074% NA no 4 −3.958 AAAATA 0.054% NA no 4 −3.325 AAAATC 0.048%NA no 4 −4.381 AAAATG 0.069% −0.216 no 4 −1.247 AAACAT 0.056% NA no 4−3.092 AAACCT 0.029%  0.310 no 4 −2.728 AAACGT 0.047%  0.294 no 4 −1.513AAACTA 0.047% NA no 4 −3.020 AAACTC 0.034% NA no 4 −2.516 AAACTG 0.046%NA no 4 −0.916 AAAGAA 0.103%  0.355 no 4 −1.592 AAAGAC 0.054%  0.390 no4 −1.483 AAAGAG 0.080% NA no 4 0.060 AAAGCA 0.066% NA no 4 −3.346 AAAGCC0.036% NA no 4 −0.725 AAAGCG 0.049%  0.309 no 4 −0.741 AAAGGA 0.084% 0.418 no 4 −1.714 AAAGGC 0.054% NA no 4 −0.894 AAAGGG 0.082% −0.263 no4 −2.890 AAATAT 0.036% −0.413 no 4 −4.350 AAATCT 0.032% NA no 4 −3.355AAATGT 0.048% NA no 4 −3.537 AAATTA 0.045% NA no 4 −5.631 AAATTC 0.024%NA no 4 −5.160 AAATTG 0.045% −0.228 no 4 −1.111 AACATT 0.036% NA no 4−1.558 AACCTT 0.022% NA no 4 −2.150 AACGAT 0.042%  0.386 no 4 0.296AACGCT 0.026%  0.361 no 4 −0.309 AACGGT 0.039% NA no 4 −0.159 AACGTA0.040% NA no 4 −0.906 AACGTC 0.032%  0.684 no 4 −0.611 AACGTG 0.037% 0.265 no 4 −0.098 AACTTT 0.022% NA no 4 −1.717 AAGATT 0.044%  0.448 no4 −0.536 AAGCTT 0.031% NA no 4 −1.965 AAGGAT 0.053%  0.567 no 4 −0.813AAGGCT 0.029% NA no 4 −3.067 AAGGGT 0.049% NA no 4 −7.986 AAGGTA 0.057%NA no 4 −5.594 AAGGTC 0.026% NA no 4 −2.533 AAGGTG 0.054% −0.162 no 4−0.085 AAGTTT 0.032% NA no 4 −2.517 AATATT 0.036% −0.315 no 4 −4.895AATCTT 0.021% NA no 4 −3.098 AATGAT 0.046% NA no 4 −2.293 AATGCT 0.024%NA no 4 −1.456 AATGGT 0.034% −0.241 no 4 −2.975 AATGTA 0.037% NA no 4−4.311 AATGTC 0.019% NA no 4 −5.201 AATGTG 0.036% NA no 4 −0.676 AATTTT0.018% NA no 4 −5.472 ACAAAT 0.060% NA no 4 −2.498 ACAACT 0.034% NA no 4−1.343 ACAAGT 0.043% NA no 4 −1.335 ACAATA 0.051% NA no 4 −2.992 ACAATC0.035% NA no 4 −2.196 ACAATG 0.044% NA no 4 −0.777 ACACAT 0.039% NA no 4−2.724 ACACCT 0.027%  0.299 no 4 −0.778 ACACGT 0.032% NA no 4 −1.097ACACTA 0.025% −0.421 no 4 −1.741 ACACTC 0.024%  0.299 no 4 −2.868 ACACTG0.034%  0.160 no 4 −0.472 ACAGAA 0.065% NA no 4 −1.632 ACAGAC 0.040% 0.393 no 4 −0.419 ACAGAG 0.050% NA no 4 −0.040 ACAGCA 0.040% NA no 4−0.830 ACAGCC 0.029% NA no 4 −0.837 ACAGCG 0.039%  0.332 no 4 0.693ACAGGA 0.059% NA no 4 −0.977 ACAGGC 0.039% NA no 4 −2.302 ACAGGG 0.053%−0.305 no 4 −3.989 ACATAT 0.038% −0.375 no 4 −3.134 ACATCT 0.026%  0.265no 4 −0.972 ACATGT 0.028% NA no 4 −1.629 ACATTA 0.038% NA no 4 −3.513ACATTC 0.024% NA no 4 −3.662 ACATTG 0.029% NA no 4 −1.130 ACCATT 0.020%NA no 4 −0.629 ACCCTT 0.011% −0.246 no 4 0.422 ACCGAT 0.022% NA no 4−0.135 ACCGCT 0.016% NA no 4 −1.150 ACCGGT 0.021% NA no 4 −0.674 ACCGTA0.024% NA no 4 −0.726 ACCGTC 0.016% NA no 4 −0.451 ACCGTG 0.023%  0.196no 4 0.271 ACCTTT 0.014% NA no 4 −2.132 ACGATT 0.031% NA no 4 −1.041ACGCTT 0.020% NA no 4 −1.397 ACGGAT 0.042%  0.588 no 4 0.238 ACGGCT0.019% NA no 4 −0.593 ACGGGT 0.038% NA no 4 −0.240 ACGGTA 0.043% NA no 4−1.121 ACGGTC 0.028%  0.541 no 4 −0.430 ACGGTG 0.022% NA no 4 −0.185ACGTTT 0.025% NA no 4 −1.488 ACTATT 0.023% −0.296 no 4 −5.484 ACTCTT0.017% NA no 4 −3.181 ACTGAT 0.025%  0.268 no 4 −1.437 ACTGCT 0.020% 0.258 no 4 −2.009 ACTGGT 0.025% NA no 4 −2.074 ACTGTA 0.032% NA no 4−2.334 ACTGTC 0.018%  0.305 no 4 −1.646 ACTGTG 0.030% NA no 4 −0.724ACTTTT 0.018% −0.426 no 4 −6.098 AGAAAA 0.098% NA no 4 −5.216 AGAAAC0.053%  0.315 no 4 −5.765 AGAAAG 0.090% NA no 4 −1.012 AGAACA 0.065% NAno 4 −5.222 AGAACC 0.041% NA no 4 −4.164 AGAACG 0.045%  0.447 no 4−2.160 AGAAGA 0.067% 1.034 no 4 −3.548 AGAAGC 0.040%  0.505 no 4 −4.989AGAAGG 0.072% NA no 4 −3.572 AGACAA 0.067% NA no 4 −2.772 AGACAC 0.034%NA no 4 −1.755 AGACAG 0.048% NA no 4 −1.138 AGACCA 0.035% NA no 4 −1.356AGACCC 0.020% NA no 4 −2.073 AGACCG 0.032%  0.453 no 4 0.067 AGACGA0.037%  0.601 no 4 −1.130 AGACGC 0.032%  0.526 no 4 −0.923 AGACGG 0.045% 0.309 no 4 −0.496 AGATAA 0.054% NA no 4 −3.790 AGATAC 0.035% NA no 4−2.669 AGATAG 0.049% −0.630 no 4 −2.242 AGATCA 0.040% NA no 4 −3.429AGATCC 0.023%  0.192 no 4 −2.733 AGATCG 0.034%  0.331 no 4 −0.645 AGATGA0.041% NA no 4 −4.270 AGATGC 0.037%  0.194 no 4 −1.573 AGATGG 0.042% NAno 4 −0.703 AGCAAT 0.044% NA no 4 −0.655 AGCACT 0.026% NA no 4 0.946AGCAGT 0.037% NA no 4 −0.523 AGCATA 0.048% NA no 4 −1.072 AGCATC 0.034%NA no 4 −0.139 AGCATG 0.033% NA no 4 0.113 AGCCAT 0.024% NA no 4 0.515AGCCCT 0.015% NA no 4 0.461 AGCCGT 0.021% NA no 4 −0.579 AGCCTA 0.022%−0.677 no 4 0.105 AGCCTC 0.019% NA no 4 −0.799 AGCCTG 0.020% NA no 40.459 AGCGAA 0.042% NA no 4 −0.480 AGCGAC 0.033%  0.462 no 4 −0.260AGCGAG 0.039% NA no 4 0.894 AGCGCA 0.032% NA no 4 −0.334 AGCGCC 0.016%NA no 4 0.702 AGCGCG 0.037%  0.413 no 4 −0.188 AGCGGA 0.047%  0.440 no 40.284 AGCGGC 0.031% NA no 4 0.786 AGCGGG 0.038%  0.181 no 4 −0.245AGCTAT 0.029% −0.338 no 4 −0.014 AGCTCT 0.017% NA no 4 −0.602 AGCTGT0.022% NA no 4 −0.424 AGCTTA 0.024% −0.405 no 4 −1.115 AGCTTC 0.018% NAno 4 0.101 AGCTTG 0.026% −0.330 no 4 −0.058 AGGAAT 0.067% NA no 4 −2.991AGGACT 0.035%  0.392 no 4 −3.459 AGGAGT 0.039% NA no 4 −1.870 AGGATA0.062% NA no 4 −7.902 AGGATC 0.035%  0.379 no 4 −4.373 AGGATG 0.052% 0.187 no 4 −5.328 AGGCAT 0.044% NA no 4 −1.828 AGGCCT 0.023% NA no 4−0.382 AGGCGT 0.034% NA no 4 −0.397 AGGCTA 0.049% −0.404 no 4 −3.324AGGCTC 0.030% NA no 4 −1.454 AGGCTG 0.030% NA no 4 0.107 AGGGAA 0.077%NA no 4 −5.306 AGGGAC 0.043% NA no 4 −6.309 AGGGAG 0.059% −0.373 no 4−2.135 AGGGCA 0.057% −0.267 no 4 −6.921 AGGGCC 0.032% −0.371 no 4 −4.173AGGGCG 0.043% −0.249 no 4 −1.496 AGGGGA 0.080% −0.275 no 4 −3.922 AGGGGC0.038% −0.225 no 4 −5.261 AGGGGG 0.065% −0.464 no 4 −3.875 AGGTAT 0.042%−0.401 no 4 −4.452 AGGTCT 0.029% NA no 4 −4.472 AGGTGT 0.037% −0.286 no4 −2.006 AGGTTA 0.047% −0.602 no 4 −3.642 AGGTTC 0.028% NA no 4 −4.493AGGTTG 0.041% −0.476 no 4 −1.140 AGTAAT 0.049% −0.394 no 4 −1.198 AGTACT0.034% NA no 4 −0.954 AGTAGT 0.035% −0.373 no 4 −3.359 AGTATA 0.055%−0.425 no 4 −1.458 AGTATC 0.031% NA no 4 −1.182 AGTATG 0.041% −0.251 no4 −0.309 AGTCAT 0.039% NA no 4 −1.017 AGTCCT 0.017% NA no 4 −0.880AGTCGT 0.024%  0.257 no 4 0.145 AGTCTA 0.035% −0.467 no 4 −0.810 AGTCTC0.020% NA no 4 1.087 AGTCTG 0.025% NA no 4 −0.660 AGTGAA 0.053% NA no 4−0.256 AGTGAC 0.025%  0.323 no 4 −0.127 AGTGAG 0.045% −0.374 no 4 −0.022AGTGCA 0.043% −0.169 no 4 −0.841 AGTGCC 0.017% NA no 4 0.818 AGTGCG0.038% NA no 4 0.561 AGTGGA 0.060% NA no 4 −0.600 AGTGGC 0.030% NA no 40.516 AGTGGG 0.047% −0.246 no 4 −0.432 AGTTAT 0.033% −0.091 no 4 −1.026AGTTCT 0.018%  0.158 no 4 −0.424 AGTTGT 0.024% NA no 4 0.336 AGTTTA0.040% −0.216 no 4 −2.315 AGTTTC 0.022%  0.254 no 4 −1.797 AGTTTG 0.026%NA no 4 0.155 ATAAAT 0.052% −0.446 yes 4 −6.581 ATAACT 0.029% −0.316 yes4 −3.848 ATAAGT 0.052% NA yes 4 −7.114 ATAATA 0.054% −0.503 yes 4 −5.864ATAATC 0.032% NA yes 4 −5.629 ATAATG 0.049% −0.335 yes 4 −4.245 ATACAT0.033% NA no 4 −3.054 ATACCT 0.018% NA no 4 −1.447 ATACGT 0.032% NA no 4−0.910 ATACTA 0.037% NA no 4 −5.216 ATACTC 0.020% NA no 4 −1.292 ATACTG0.033% NA no 4 −0.298 ATAGAA 0.053% NA yes 4 −8.271 ATAGAC 0.031% NA yes4 −8.524 ATAGAG 0.049% −0.265 yes 4 −3.258 ATAGCA 0.040% −0.383 yes 4−7.504 ATAGCC 0.018% −0.279 yes 4 −5.802 ATAGCG 0.040% NA yes 4 −4.412ATAGGA 0.047% NA yes 4 −6.413 ATAGGC 0.021% NA yes 4 −5.793 ATAGGG0.044% −0.698 yes 4 −8.103 ATATAT 0.034% −0.374 no 4 −3.377 ATATCT0.027% NA no 4 −3.044 ATATGT 0.034% NA no 4 −3.775 ATATTA 0.045% −0.360no 4 −3.798 ATATTC 0.024% NA no 4 −5.407 ATATTG 0.041% −0.328 no 4−1.972 ATCATT 0.028% NA no 4 0.861 ATCCTT 0.019% NA no 4 0.264 ATCGAT0.034%  0.312 no 4 −0.464 ATCGCT 0.021% NA no 4 0.221 ATCGGT 0.032% NAno 4 0.601 ATCGTA 0.032% NA no 4 0.152 ATCGTC 0.020%  0.652 no 4 −0.624ATCGTG 0.032%  0.214 no 4 −0.159 ATCTTT 0.018% NA no 4 −0.768 ATGATT0.040% NA yes 4 −4.782 ATGCTT 0.025% NA no 4 −2.106 ATGGAT 0.042%  0.299no 4 −0.973 ATGGCT 0.027% NA no 4 −0.920 ATGGGT 0.042% −0.494 no 4−4.650 ATGGTA 0.043% −0.484 no 4 −3.345 ATGGTC 0.035% NA no 4 −3.585ATGGTG 0.038% −0.148 no 4 −0.300 ATGTTT 0.030% NA no 4 −3.404 ATTATT0.025% −0.286 no 4 −4.186 ATTCTT 0.018% −0.283 no 4 −3.950 ATTGAT 0.039%NA no 4 −2.368 ATTGCT 0.018% −0.110 no 4 −3.597 ATTGGT 0.033% NA no 4−1.753 ATTGTA 0.037% −0.367 no 4 −3.645 ATTGTC 0.019% NA no 4 −4.034ATTGTG 0.030% −0.157 no 4 −0.111 ATTTTT 0.020% −0.599 no 4 −6.439 CAAAAT0.035% −0.265 no 4 −1.870 CAAACT 0.026% NA no 4 −1.080 CAAAGT 0.031% NAno 4 −1.396 CAAATA 0.026% −0.390 no 4 −2.759 CAAATC 0.020% NA no 4−1.123 CAAATG 0.032% NA no 4 0.408 CAACAT 0.027%  0.196 no 4 −1.648CAACCT 0.013%  0.189 no 4 −0.682 CAACGT 0.017%  0.414 no 4 −0.326 CAACTA0.018% NA no 4 −0.869 CAACTC 0.012%  0.284 no 4 −1.207 CAACTG 0.022% 0.270 no 4 1.389 CAAGAA 0.041%  0.922 no 4 −0.995 CAAGAC 0.020%  0.705no 4 −0.250 CAAGAG 0.031%  0.411 no 4 0.703 CAAGCA 0.026% NA no 4 −1.164CAAGCC 0.016% NA no 4 −0.329 CAAGCG 0.021%  0.353 no 4 1.237 CAAGGA0.038%  0.620 no 4 −0.511 CAAGGC 0.021%  0.209 no 4 −1.030 CAAGGG 0.034%NA no 4 −0.664 CAATAT 0.020% −0.268 no 4 −2.422 CAATCT 0.014% NA no 41.219 CAATGT 0.019% NA no 4 −0.901 CAATTA 0.024% −0.483 no 4 −1.901CAATTG 0.015% NA no 4 0.420 CACATT 0.014% NA no 4 3.185 CACCTT 0.009%−0.286 no 4 −1.341 CACGAT 0.023% NA no 4 −0.362 CACGCT 0.010% NA no 4−0.082 CACGGT 0.019% NA no 4 −0.840 CACGTA 0.021% −0.253 no 4 −0.043CACGTC 0.010%  0.302 no 4 0.755 CACGTG 0.014% NA no 4 0.005 CACTTT0.013% −0.551 no 4 0.538 CAGATT 0.024% NA no 4 −2.078 CAGCTT 0.017%−0.379 no 4 −0.713 CAGGAT 0.029% NA no 4 −0.515 CAGGCT 0.020% −0.217 no4 −3.261 CAGGGT 0.031% −0.438 no 4 −5.036 CAGGTA 0.030% −0.604 no 4−4.058 CAGGTC 0.016% −0.283 no 4 −3.073 CAGGTG 0.028% −0.405 no 4 −1.431CAGTTT 0.017% −0.231 no 4 −1.048 CATATT 0.013% −0.298 no 4 −3.047 CATCTT0.009% −0.255 no 4 −0.392 CATGAT 0.021% NA no 4 −1.500 CATGCT 0.015% NAno 4 1.442 CATGGT 0.018% NA no 4 −1.403 CATGTA 0.021% −0.228 no 4 −1.773CATGTC 0.011% NA no 4 −3.145 CATGTG 0.017% NA no 4 1.066 CATTTT 0.013%−0.488 no 4 −5.269 CCAAAT 0.018% −0.435 no 4 −2.137 CCAACT 0.017% NA no4 −1.663 CCAAGT 0.020% NA no 4 −1.211 CCAATA 0.020% −0.660 no 4 −2.066CCAATC 0.016% −0.206 no 4 −2.827 CCAATG 0.019% NA no 4 −0.077 CCACAT0.018% NA no 4 −1.707 CCACCT 0.013% −0.247 no 4 −1.130 CCACGT 0.013% 0.193 no 4 −0.068 CCACTA 0.015% −0.448 no 4 −1.820 CCACTC 0.011% NA no4 −1.964 CCACTG 0.013% NA no 4 −0.784 CCAGAA 0.031% NA no 4 −1.968CCAGAC 0.018% −0.293 no 4 0.897 CCAGAG 0.023% NA no 4 −0.694 CCAGCA0.020% −0.894 no 4 0.249 CCAGCC 0.010% −0.361 no 4 −0.074 CCAGCG 0.016%NA no 4 0.296 CCAGGA 0.023% NA no 4 −0.226 CCAGGC 0.014% NA no 4 0.094CCAGGG 0.023% −0.081 no 4 −0.517 CCATAT 0.014% −0.454 no 4 −4.374 CCATCT0.011% NA no 4 −1.363 CCATGT 0.011% NA no 4 −0.157 CCATTA 0.017% −0.770no 4 −1.677 CCATTC 0.009% NA no 4 −0.177 CCATTG 0.011% NA no 4 −1.246CCCATT 0.007% −0.354 no 4 −1.982 CCCCTT 0.005% −0.393 no 4 −3.756 CCCGAT0.013% NA no 4 −0.672 CCCGCT 0.012%  0.270 no 4 −1.878 CCCGGT 0.007% 0.115 no 4 −0.464 CCCGTA 0.010% −0.151 no 4 0.711 CCCGTC 0.006%  0.533no 4 −0.470 CCCGTG 0.009%  0.323 no 4 2.700 CCCTTT 0.007% −0.551 no 4−1.067 CCGATT 0.016% NA no 4 0.036 CCGCTT 0.007% NA no 4 1.319 CCGGAT0.018%  0.357 no 4 −0.103 CCGGCT 0.012% NA no 4 0.454 CCGGGT 0.015% NAno 4 −0.140 CCGGTA 0.015% NA no 4 −1.501 CCGGTC 0.008%  0.221 no 4 0.045CCGGTG 0.012%  0.134 no 4 −0.901 CCGTTT 0.008% NA no 4 −0.313 CCTATT0.006% −0.520 no 4 −0.699 CCTCTT 0.007% −0.371 no 4 −1.879 CCTGAT 0.015%NA no 4 −0.602 CCTGCT 0.013%  0.416 no 4 −0.136 CCTGGT 0.011% NA no 40.693 CCTGTA 0.007% −0.279 no 4 −0.935 CCTGTC 0.011% NA no 4 −0.597CCTGTG 0.012%  0.149 no 4 −0.177 CCTTTT 0.005% −0.777 no 4 −3.580 CGAAAA0.031% NA no 4 −0.325 CGAAAC 0.019%  0.331 no 4 2.952 CGAAAG 0.030% NAno 4 −0.310 CGAACA 0.028% NA no 4 −0.344 CGAACC 0.018%  0.405 no 4−0.518 CGAACG 0.028%  0.614 no 4 0.655 CGAAGA 0.026%  0.750 no 4 −0.446CGAAGC 0.016%  0.640 no 4 −1.093 CGAAGG 0.042%  0.274 no 4 −0.938 CGACAA0.018% NA no 4 1.181 CGACAC 0.020% NA no 4 −0.391 CGACAG 0.021% NA no 40.596 CGACCA 0.018%  0.529 no 4 0.429 CGACCC 0.011%  0.219 no 4 −2.014CGACCG 0.016%  0.578 no 4 0.463 CGACGA 0.015%  0.805 no 4 −0.028 CGACGC0.011%  0.740 no 4 −0.538 CGACGG 0.013%  0.825 no 4 −0.848 CGATAA 0.020%NA no 4 0.330 CGATAC 0.018% NA no 4 −1.775 CGATAG 0.018% −0.372 no 40.689 CGATCA 0.018% NA no 4 −0.304 CGATCC 0.009%  0.447 no 4 0.031CGATCG 0.014%  0.517 no 4 0.830 CGATGA 0.017%  0.512 no 4 −0.894 CGATGC0.014%  0.283 no 4 −0.550 CGATGG 0.018%  0.422 no 4 0.218 CGCAAT 0.007%NA no 4 −0.769 CGCACT 0.014% NA no 4 −0.908 CGCAGT 0.013% NA no 4 0.009CGCATA 0.013% NA no 4 0.526 CGCATC 0.012%  0.410 no 4 −0.491 CGCATG0.015% NA no 4 −0.422 CGCCAT 0.013% NA no 4 0.443 CGCCCT 0.007%  0.299no 4 0.095 CGCCGT 0.010%  0.479 no 4 −1.365 CGCCTA 0.012% NA no 4 0.513CGCCTC 0.005% NA no 4 −1.467 CGCCTG 0.007%  0.445 no 4 −1.598 CGCGAA0.021%  0.542 no 4 0.075 CGCGAC 0.009%  0.747 no 4 2.830 CGCGAG 0.014% 0.503 no 4 −0.598 CGCGCA 0.016%  0.350 no 4 −1.400 CGCGCC 0.006%  0.622no 4 0.969 CGCGCG 0.013%  0.725 no 4 −0.929 CGCGGA 0.017%  0.784 no 40.208 CGCGGC 0.009% NA no 4 1.168 CGCGGG 0.016%  0.640 no 4 0.489 CGCTAT0.010% NA no 4 0.803 CGCTCT 0.009% NA no 4 −0.502 CGCTGT 0.008%  0.248no 4 0.701 CGCTTA 0.013% NA no 4 −0.500 CGCTTC 0.006%  0.397 no 4 −0.684CGCTTG 0.010% NA no 4 0.365 CGGAAT 0.022%  0.487 no 4 0.037 CGGACT0.018%  0.444 no 4 1.943 CGGAGT 0.022%  0.430 no 4 −0.112 CGGATA 0.024%NA no 4 0.093 CGGATC 0.010%  0.439 no 4 −0.003 CGGATG 0.023%  0.573 no 40.003 CGGCAT 0.016% NA no 4 −0.147 CGGCCT 0.007% NA no 4 0.935 CGGCGT0.013%  0.570 no 4 −1.007 CGGCTA 0.014% NA no 4 0.336 CGGCTC 0.012% NAno 4 1.684 CGGCTG 0.013%  0.249 no 4 −0.227 CGGGAA 0.029%  0.392 no 40.280 CGGGAC 0.020%  0.486 no 4 −0.590 CGGGAG 0.029%  0.496 no 4 −0.051CGGGCA 0.025%  0.387 no 4 −0.248 CGGGCC 0.011%  0.242 no 4 0.006 CGGGCG0.021%  0.335 no 4 −1.589 CGGGGA 0.032%  0.320 no 4 −0.896 CGGGGC 0.015% 0.291 no 4 0.341 CGGGGG 0.026%  0.102 no 4 0.833 CGGTAT 0.015% NA no 41.168 CGGTCT 0.009%  0.261 no 4 0.198 CGGTTA 0.017% NA no 4 −0.187CGGTTC 0.007%  0.358 no 4 −1.306 CGGTTG 0.013% NA no 4 −0.579 CGTAAT0.017% NA no 4 0.298 CGTACT 0.009% NA no 4 −1.035 CGTAGT 0.011% NA no 41.330 CGTATA 0.017% NA no 4 −0.144 CGTATC 0.011% NA no 4 0.476 CGTATG0.011% NA no 4 1.448 CGTCAT 0.008%  0.367 no 4 0.543 CGTCCT 0.005% 0.477 no 4 −0.983 CGTCGT 0.006%  0.685 no 4 0.655 CGTCTA 0.010% NA no 4−0.340 CGTCTC 0.006%  0.353 no 4 −1.327 CGTCTG 0.012%  0.574 no 4 0.286CGTGAA 0.022%  0.406 no 4 −1.418 CGTGAC 0.011%  0.488 no 4 2.362 CGTGAG0.015% NA no 4 −0.829 CGTGCA 0.018%  0.186 no 4 0.425 CGTGCC 0.011% 0.437 no 4 0.169 CGTGCG 0.015%  0.538 no 4 −0.486 CGTGGA 0.014%  0.693no 4 −1.367 CGTGGC 0.010%  0.436 no 4 4.292 CGTGGG 0.018%  0.366 no 4−0.381 CGTTAT 0.012% NA no 4 −2.301 CGTTGT 0.007% NA no 4 1.554 CGTTTA0.010% NA no 4 −0.902 CGTTTC 0.008% NA no 4 −1.057 CGTTTG 0.007% NA no 4−0.386 CTAAAT 0.016% −0.493 yes 4 −4.226 CTAACT 0.011% −0.371 yes 4−3.767 CTAAGT 0.015% −0.515 yes 4 −5.028 CTAATA 0.012% −0.705 yes 4−5.432 CTAATC 0.010% NA yes 4 −3.637 CTAATG 0.015% −0.382 yes 4 −2.958CTACAT 0.007% NA no 4 1.999 CTACCT 0.004% NA no 4 −0.421 CTACGT 0.010% 0.348 no 4 0.615 CTACTA 0.008% NA no 4 −1.895 CTACTC 0.009% NA no 4−0.966 CTACTG 0.005%  0.182 no 4 −0.861 CTAGAA 0.015% NA yes 4 −5.617CTAGAC 0.011% −0.350 yes 4 −4.679 CTAGAG 0.011% −0.315 yes 4 −3.370CTAGCA 0.012% −0.848 yes 4 −6.462 CTAGCC 0.005% −0.415 yes 4 −2.428CTAGCG 0.008% NA yes 4 −3.916 CTAGGA 0.015% NA yes 4 −3.358 CTAGGC0.010% −0.457 yes 4 −5.406 CTAGGG 0.015% −0.600 yes 4 −7.655 CTATAT0.008% −0.636 no 4 −2.937 CTATCT 0.005% NA no 4 −4.321 CTATGT 0.009%−0.307 no 4 −2.655 CTATTA 0.010% −0.634 no 4 −2.367 CTATTC 0.009% −0.292no 4 −3.078 CTATTG 0.009% −0.357 no 4 −1.023 CTCCTT 0.006% NA no 4 0.943CTCGAT 0.008%  0.285 no 4 0.153 CTCGCT 0.008% NA no 4 1.062 CTCGTA0.013% NA no 4 −1.622 CTCGTC 0.008%  0.486 no 4 0.350 CTCGTG 0.009% 0.250 no 4 −0.417 CTCTTT 0.007% −0.352 no 4 0.105 CTGATT 0.011% NA yes4 −4.011 CTGCTT 0.010% NA no 4 1.029 CTGGAT 0.013%  0.434 no 4 1.593CTGGCT 0.010% NA no 4 1.129 CTGGGT 0.011% NA no 4 0.004 CTGGTA 0.014%−0.388 no 4 0.522 CTGGTC 0.007% NA no 4 1.659 CTGGTG 0.009% NA no 4−0.709 CTGTTT 0.008% NA no 4 −0.953 CTTCTT 0.006% −0.279 no 4 −1.950CTTGAT 0.012% NA no 4 1.198 CTTGGT 0.010% NA no 4 −0.218 CTTGTA 0.010%−0.365 no 4 −2.510 CTTGTC 0.005% NA no 4 −2.410 CTTGTG 0.008% NA no 40.217 CTTTTT 0.006% −0.780 no 4 −5.717 GAAAAT 0.049% NA no 4 −1.270GAAACT 0.048%  0.383 no 4 −1.006 GAAAGT 0.053% NA no 4 −2.007 GAAATA0.036% NA no 4 −1.518 GAAATC 0.033%  0.426 no 4 −2.935 GAAATG 0.053% NAno 4 −0.642 GAACAT 0.044%  0.361 no 4 −1.180 GAACCT 0.024%  0.566 no 4−0.178 GAACGT 0.038%  0.508 no 4 −0.118 GAACTA 0.038% NA no 4 −0.585GAACTC 0.021%  0.348 no 4 −0.898 GAACTG 0.038%  0.477 no 4 0.027 GAAGAA0.068%  0.845 no 4 −0.634 GAAGAC 0.038%  0.964 no 4 −0.261 GAAGAG 0.073% 0.490 no 4 −0.123 GAAGCA 0.058%  0.357 no 4 −0.302 GAAGCC 0.032%  0.598no 4 −0.252 GAAGCG 0.045%  0.556 no 4 −0.199 GAAGGA 0.066%  0.565 no 40.084 GAAGGC 0.046%  0.553 no 4 −0.739 GAAGGG 0.069% NA no 4 −1.285GAATAT 0.033% NA no 4 −2.215 GAATCT 0.027%  0.354 no 4 −1.541 GAATGT0.045% NA no 4 −1.735 GAATTA 0.044% NA no 4 −1.820 GAATTC 0.020%  0.350no 4 −2.628 GAATTG 0.039%  0.142 no 4 −0.239 GACATT 0.026%  0.245 no 4−1.062 GACCTT 0.017%  0.438 no 4 −2.298 GACGAT 0.036%  0.760 no 4 −0.060GACGCT 0.022%  0.544 no 4 −0.296 GACGGT 0.024%  0.405 no 4 1.144 GACGTA0.030%  0.372 no 4 −0.589 GACGTC 0.019%  0.984 no 4 1.098 GACGTG 0.035% 0.487 no 4 0.160 GACTTT 0.018% NA no 4 −0.754 GAGATT 0.031%  0.237 no 4−1.633 GAGCTT 0.023% NA no 4 0.449 GAGGAT 0.049%  0.531 no 4 −0.571GAGGCT 0.031% NA no 4 0.152 GAGGGT 0.032% −0.340 no 4 −6.092 GAGGTA0.047% −0.287 no 4 −3.978 GAGGTC 0.022%  0.262 no 4 −1.787 GAGGTG 0.041%NA no 4 −0.762 GAGTTT 0.031% NA no 4 −1.716 GATATT 0.031% NA no 4 −2.944GATCTT 0.015% NA no 4 −0.802 GATGAT 0.035%  0.456 no 4 −1.235 GATGCT0.013%  0.262 no 4 −0.287 GATGGT 0.026% NA no 4 −1.077 GATGTA 0.028% NAno 4 −1.822 GATGTC 0.023%  0.521 no 4 −0.002 GATGTG 0.026% NA no 4−0.720 GATTTT 0.023% NA no 4 −3.296 GCAAAT 0.035% NA no 4 −1.702 GCAACT0.023%  0.248 no 4 −0.187 GCAAGT 0.036%  0.245 no 4 −0.425 GCAATA 0.032%−0.178 no 4 −1.745 GCAATC 0.019%  0.247 no 4 −1.903 GCAATG 0.036%  0.107no 4 −0.278 GCACAT 0.026% −0.166 no 4 −1.646 GCACCT 0.020% −0.246 no 4−0.666 GCACGT 0.027% NA no 4 −0.048 GCACTA 0.027% −0.331 no 4 −2.294GCACTC 0.018% −0.183 no 4 −1.563 GCACTG 0.019% NA no 4 −0.601 GCAGAA0.038%  0.343 no 4 −6.925 GCAGAC 0.035%  0.271 no 4 −2.639 GCAGAG 0.036%NA no 4 −1.011 GCAGCA 0.039%  0.120 no 4 −0.720 GCAGCC 0.018% −0.320 no4 −1.494 GCAGCG 0.030%  0.204 no 4 −1.455 GCAGGA 0.044%  0.120 no 4−2.136 GCAGGC 0.029% NA no 4 −1.642 GCAGGG 0.045% −0.272 no 4 −3.944GCATAT 0.025% NA no 4 −1.368 GCATCT 0.015% −0.139 no 4 −0.114 GCATGT0.026% NA no 4 −1.883 GCATTA 0.028% −0.261 no 4 −2.675 GCATTC 0.017% NAno 4 −2.250 GCATTG 0.022% NA no 4 −0.636 GCCATT 0.014% −0.318 no 4−0.142 GCCCTT 0.011% −0.247 no 4 4.529 GCCGAT 0.019% NA no 4 0.211GCCGCT 0.011% NA no 4 −0.760 GCCGGT 0.019% NA no 4 0.710 GCCGTA 0.018%NA no 4 −1.313 GCCGTC 0.013%  0.485 no 4 0.306 GCCGTG 0.017%  0.215 no 4−0.949 GCCTTT 0.012% −0.405 no 4 0.054 GCGATT 0.020% NA no 4 0.051GCGCTT 0.015% NA no 4 −0.932 GCGGAT 0.033%  0.541 no 4 −0.771 GCGGCT0.022% NA no 4 0.004 GCGGGT 0.022% NA no 4 −2.285 GCGGTA 0.029% NA no 4−0.965 GCGGTC 0.016%  0.359 no 4 1.092 GCGGTG 0.021% NA no 4 0.297GCGTTT 0.013% NA no 4 1.112 GCTATT 0.009% −0.350 no 4 −0.895 GCTCTT0.011% −0.258 no 4 −0.708 GCTGAT 0.018% NA no 4 −0.478 GCTGCT 0.011% 0.337 no 4 1.276 GCTGGT 0.017% NA no 4 −0.001 GCTGTA 0.021% NA no 4−0.812 GCTGTC 0.012%  0.466 no 4 0.824 GCTGTG 0.022% NA no 4 −0.104GCTTTT 0.019% −0.329 no 4 −3.786 GGAAAA 0.078% NA no 4 −0.519 GGAAAC0.058%  0.455 no 4 −0.299 GGAAAG 0.073% NA no 4 −0.182 GGAACA 0.056% 0.415 no 4 −0.135 GGAACC 0.031%  0.593 no 4 0.121 GGAACG 0.058%  0.522no 4 0.398 GGAAGA 0.070%  0.651 no 4 0.217 GGAAGC 0.041%  0.486 no 40.471 GGAAGG 0.063% NA no 4 −0.272 GGACAA 0.065%  0.466 no 4 −0.825GGACAC 0.039%  0.516 no 4 0.198 GGACAG 0.052% NA no 4 −0.415 GGACCA0.034%  0.364 no 4 −0.509 GGACCC 0.022%  0.372 no 4 0.013 GGACCG 0.029% 0.636 no 4 0.962 GGACGA 0.041%  0.697 no 4 0.739 GGACGC 0.034%  0.761no 4 −0.271 GGACGG 0.034%  0.396 no 4 0.562 GGATAA 0.063% NA no 4 0.416GGATAC 0.039%  0.426 no 4 0.494 GGATAG 0.052% −0.376 no 4 −0.358 GGATCA0.037%  0.194 no 4 0.022 GGATCC 0.020%  0.445 no 4 −0.093 GGATCG 0.031% 0.388 no 4 1.722 GGATGA 0.049%  0.391 no 4 −0.001 GGATGC 0.029%  0.417no 4 0.427 GGATGG 0.047% NA no 4 −0.240 GGCAAT 0.028%  0.112 no 4 −0.483GGCACT 0.020% −0.251 no 4 0.601 GGCAGT 0.050% −0.107 no 4 −0.032 GGCATA0.027% NA no 4 −0.266 GGCATC 0.016% NA no 4 0.824 GGCATG 0.020%  0.074no 4 −0.492 GGCCAT 0.019% NA no 4 −0.309 GGCCCT 0.012% NA no 4 2.149GGCCGT 0.015% NA no 4 −0.527 GGCCTA 0.016% −0.260 no 4 0.274 GGCCTC0.011% NA no 4 0.063 GGCCTG 0.018%  0.128 no 4 −0.511 GGCGAA 0.038% 0.405 no 4 0.166 GGCGAC 0.024%  0.608 no 4 0.471 GGCGAG 0.030%  0.169no 4 0.217 GGCGCA 0.027%  0.299 no 4 1.041 GGCGCC 0.011%  0.480 no 40.303 GGCGCG 0.023%  0.455 no 4 −0.923 GGCGGA 0.034%  0.499 no 4 −0.059GGCGGC 0.021%  0.302 no 4 −1.131 GGCGGG 0.033%  0.148 no 4 0.621 GGCTAT0.021% −0.223 no 4 0.232 GGCTCT 0.016% −0.222 no 4 0.361 GGCTGT 0.021% 0.169 no 4 1.237 GGCTTA 0.021% −0.295 no 4 0.226 GGCTTC 0.009%  0.251no 4 −0.796 GGCTTG 0.016% −0.193 no 4 0.210 GGGAAT 0.063% NA no 4 −0.739GGGACT 0.038% NA no 4 0.251 GGGAGT 0.043% NA no 4 0.533 GGGATA 0.049% NAno 4 −0.751 GGGATC 0.024% NA no 4 1.275 GGGATG 0.052% NA no 4 −0.042GGGCAT 0.041% −0.190 no 4 −0.624 GGGCCT 0.018% NA no 4 −0.153 GGGCGT0.024% NA no 4 0.901 GGGCTA 0.033% −0.444 no 4 0.594 GGGCTC 0.018%−0.236 no 4 0.395 GGGCTG 0.029% NA no 4 0.530 GGGGAA 0.067% −0.337 no 4−0.749 GGGGAC 0.034% NA no 4 0.050 GGGGAG 0.053% −0.073 no 4 0.293GGGGCA 0.048% −0.080 no 4 −0.674 GGGGCC 0.019% −0.206 no 4 −1.051 GGGGCG0.029% −0.237 no 4 −0.037 GGGGGA 0.059% −0.232 no 4 −1.399 GGGGGC 0.032%−0.277 no 4 −0.109 GGGGGG 0.043% −0.358 no 4 −4.336 GGGTAT 0.048% −0.508no 4 −0.700 GGGTCT 0.019% −0.347 no 4 −0.111 GGGTGT 0.027% −0.392 no 4−0.589 GGGTTA 0.031% −0.737 no 4 −1.798 GGGTTC 0.022% NA no 4 −0.140GGGTTG 0.034% −0.472 no 4 −0.592 GGTAAT 0.043% −0.489 no 4 −0.439 GGTACT0.023% −0.215 no 4 0.632 GGTAGT 0.035% −0.612 no 4 −0.599 GGTATA 0.040%−0.540 no 4 0.227 GGTATC 0.023% NA no 4 0.044 GGTATG 0.036% −0.317 no 40.528 GGTCAT 0.032% NA no 4 −0.896 GGTCCT 0.016% NA no 4 −1.892 GGTCGT0.020% NA no 4 0.208 GGTCTA 0.020% −0.305 no 4 −1.591 GGTCTC 0.015% NAno 4 0.749 GGTCTG 0.027% NA no 4 −0.024 GGTGAA 0.050% NA no 4 0.240GGTGAC 0.027%  0.200 no 4 0.088 GGTGAG 0.033% −0.416 no 4 −0.066 GGTGCA0.030% −0.150 no 4 0.432 GGTGCC 0.015% NA no 4 −1.141 GGTGCG 0.023% NAno 4 −0.078 GGTGGA 0.032% NA no 4 0.676 GGTGGC 0.025% −0.350 no 4 −0.348GGTGGG 0.033% −0.359 no 4 0.100 GGTTAT 0.026% −0.434 no 4 −0.053 GGTTGT0.019% −0.427 no 4 −0.566 GGTTTA 0.025% −0.700 no 4 −1.313 GGTTTC 0.015%NA no 4 −0.270 GTAAAT 0.039% −0.450 yes 4 −5.587 GTAACT 0.028% −0.326yes 4 −8.508 GTAAGT 0.036% −0.569 yes 4 −8.380 GTAATA 0.034% −0.538 yes4 −4.998 GTAATC 0.021% −0.264 yes 4 −4.319 GTAATG 0.041% −0.313 yes 4−3.064 GTACAT 0.027% −0.249 no 4 −2.516 GTACCT 0.014% NA no 4 −1.269GTACGT 0.025% NA no 4 −1.743 GTACTA 0.018% −0.479 no 4 −2.948 GTACTC0.013% NA no 4 −2.897 GTACTG 0.020% NA no 4 −1.301 GTAGAA 0.046% −0.357yes 4 −7.153 GTAGAC 0.020% NA yes 4 −7.542 GTAGAG 0.039% −0.393 yes 4−3.410 GTAGCA 0.037% −0.466 yes 4 −4.915 GTAGCC 0.018% −0.537 yes 4−7.972 GTAGCG 0.031% NA yes 4 −4.069 GTAGGA 0.033% −0.351 yes 4 −6.807GTAGGC 0.022% −0.566 yes 4 −6.937 GTAGGG 0.035% −0.733 yes 4 −8.788GTATAT 0.026% −0.383 no 4 −3.147 GTATCT 0.013% −0.249 no 4 −4.117 GTATGT0.024% −0.335 no 4 −1.977 GTATTA 0.031% −0.755 no 4 −3.084 GTATTC 0.018%NA no 4 −4.031 GTATTG 0.030% −0.271 no 4 −0.604 GTCATT 0.014% NA no 4−0.130 GTCCTT 0.008% NA no 4 −0.271 GTCGAT 0.018% NA no 4 1.936 GTCGCT0.016% NA no 4 −0.815 GTCGGT 0.020% NA no 4 −1.066 GTCGTA 0.023% NA no 4−0.555 GTCGTC 0.012%  0.774 no 4 −1.239 GTCGTG 0.022%  0.263 no 4 −0.507GTCTTT 0.012% −0.243 no 4 −0.916 GTGATT 0.025% NA yes 4 −3.033 GTGCTT0.016% −0.416 no 4 −1.320 GTGGAT 0.034%  0.389 no 4 −0.576 GTGGCT 0.024%NA no 4 0.805 GTGGGT 0.037% −0.337 no 4 −2.621 GTGGTA 0.033% −0.223 no 4−0.949 GTGGTC 0.022% NA no 4 −0.247 GTGGTG 0.029% NA no 4 −1.036 GTGTTT0.025% −0.267 no 4 −1.785 GTTATT 0.023% −0.254 no 4 −4.384 GTTCTT 0.011%NA no 4 −2.936 GTTGAT 0.031% NA no 4 −1.551 GTTGCT 0.013% NA no 4 −5.537GTTGGT 0.019% −0.158 no 4 −0.195 GTTGTA 0.026% −0.157 no 4 −2.294 GTTGTC0.010%  0.267 no 4 −0.361 GTTGTG 0.026% −0.109 no 4 −1.123 GTTTTT 0.019%−0.256 no 4 −4.352 TAAAAA 0.052% −0.365 no 4 −4.607 TAAAAC 0.044% −0.380no 4 −5.540 TAAAAG 0.048% −0.310 no 4 −0.877 TAAACA 0.051% NA no 4−5.134 TAAACC 0.026% −0.306 no 4 −3.324 TAAACG 0.038% NA no 4 −0.381TAAAGA 0.048% NA no 4 −5.819 TAAAGC 0.031% NA no 4 −2.365 TAAAGG 0.048%−0.407 no 4 −2.467 TAACAA 0.044% NA no 4 −4.893 TAACAC 0.025% NA no 4−3.223 TAACAG 0.038% −0.436 no 4 −2.106 TAACCA 0.022% −0.233 no 4 −3.482TAACCC 0.018% −0.442 no 4 −5.544 TAACCG 0.026%  0.286 no 4 −0.202 TAACGA0.030% NA no 4 −2.567 TAACGC 0.024% NA no 4 −2.384 TAACGG 0.032% NA no 4−0.389 TAATAA 0.032% −0.491 no 4 −4.881 TAATAC 0.021% −0.299 no 4 −4.682TAATAG 0.031% −0.647 no 4 −4.229 TAATCA 0.026% NA no 4 −4.280 TAATCC0.010% −0.266 no 4 −2.751 TAATCG 0.027% NA no 4 −1.773 TAATGA 0.029% NAno 4 −4.909 TAATGC 0.025% −0.398 no 4 −4.292 TAATGG 0.026% −0.300 no 4−2.506 TACAAT 0.022% −0.257 no 4 −1.284 TACACT 0.020% NA no 4 −1.208TACAGT 0.022% −0.265 no 4 −0.749 TACATA 0.018% NA no 4 −1.980 TACATC0.015%  0.314 no 4 −1.724 TACATG 0.014% −0.190 no 4 1.238 TACCAT 0.014%NA no 4 −0.613 TACCGT 0.014% NA no 4 0.179 TACCTA 0.007% NA no 4 −0.056TACCTC 0.006% NA no 4 −1.598 TACCTG 0.010%  0.337 no 4 −2.466 TACGAA0.028% NA no 4 −0.365 TACGAC 0.016%  0.542 no 4 −0.568 TACGAG 0.021% NAno 4 −0.315 TACGCA 0.021% NA no 4 0.237 TACGCC 0.010%  0.354 no 4 1.754TACGCG 0.016%  0.546 no 4 −0.239 TACGGA 0.021%  0.425 no 4 −0.398 TACGGC0.016%  0.391 no 4 1.082 TACGGG 0.028%  0.230 no 4 −0.753 TACTAT 0.013%−0.249 no 4 −1.412 TACTCT 0.008% NA no 4 −2.017 TACTGT 0.013% NA no 4−1.244 TACTTA 0.012% −0.475 no 4 −3.824 TACTTC 0.014% NA no 4 −1.406TACTTG 0.008% −0.255 no 4 −1.427 TAGAAT 0.029% −0.419 no 4 −4.933 TAGACT0.016% NA no 4 −2.457 TAGAGT 0.027% −0.406 no 4 −5.672 TAGATA 0.028%−0.861 no 4 −7.189 TAGATC 0.010% NA no 4 −7.528 TAGATG 0.030% −0.328 no4 −3.495 TAGCAT 0.021% −0.499 no 4 −6.178 TAGCCT 0.010% −0.266 no 4−5.320 TAGCGT 0.019% −0.344 no 4 −2.887 TAGCTA 0.016% −0.812 no 4 −7.930TAGCTC 0.008% −0.436 no 4 −5.048 TAGCTG 0.016% −0.306 no 4 −2.301 TAGGAA0.034% −0.600 no 4 −6.755 TAGGAC 0.021% NA no 4 −7.387 TAGGAG 0.028%−0.464 no 4 −3.571 TAGGCA 0.018% −0.835 no 4 −7.713 TAGGCC 0.011% −0.517no 4 −5.906 TAGGCG 0.019% −0.387 no 4 −3.855 TAGGGA 0.031% −0.838 no 4−9.429 TAGGGC 0.021% −0.635 no 4 −9.433 TAGGGG 0.030% −0.659 no 4 −6.441TAGTAT 0.021% −0.723 no 4 −6.245 TAGTCT 0.013% −0.369 no 4 −7.485 TAGTGT0.021% −0.579 no 4 −5.277 TAGTTA 0.019% −0.893 no 4 −7.370 TAGTTC 0.013%−0.509 no 4 −6.180 TAGTTG 0.016% −0.692 no 4 −5.193 TATAAT 0.033% −0.595no 4 −5.470 TATACT 0.019% NA no 4 −2.988 TATAGT 0.023% −0.551 no 4−5.083 TATATA 0.027% −0.586 no 4 −5.232 TATATC 0.019% NA no 4 −8.641TATATG 0.021% −0.443 no 4 −1.371 TATCAT 0.021% NA no 4 −6.799 TATCCT0.008% NA no 4 −1.638 TATCGT 0.015% NA no 4 −0.464 TATCTA 0.016% NA no 4−2.487 TATCTC 0.013% NA no 4 −3.535 TATCTG 0.015% NA no 4 −0.043 TATGAA0.035% NA no 4 −3.180 TATGAC 0.019% NA no 4 −3.071 TATGAG 0.033% −0.294no 4 −0.513 TATGCA 0.027% −0.299 no 4 −3.824 TATGCC 0.010% NA no 4−2.631 TATGCG 0.022% NA no 4 −0.008 TATGGA 0.032% NA no 4 −0.571 TATGGC0.027% NA no 4 −2.052 TATGGG 0.017% −0.217 no 4 −2.241 TATTAT 0.024%−0.434 no 4 −5.274 TATTCT 0.010% NA no 4 −3.611 TATTGT 0.024% −0.361 no4 −2.956 TATTTA 0.022% −0.674 no 4 −7.627 TATTTC 0.011% −0.407 no 4−3.981 TATTTG 0.020% −0.421 no 4 −2.248 TCAAAA 0.040% NA no 4 −3.057TCAAAC 0.027% NA no 4 −1.499 TCAAAG 0.041% NA no 4 −0.991 TCAACA 0.034%NA no 4 −1.340 TCAACC 0.017%  0.222 no 4 −0.613 TCAACG 0.021%  0.643 no4 −0.347 TCAAGA 0.038%  0.464 no 4 −0.818 TCAAGC 0.027%  0.356 no 4−1.126 TCAAGG 0.036% NA no 4 −1.564 TCACAA 0.028% NA no 4 −2.351 TCACAC0.019% NA no 4 −1.523 TCACAG 0.024% −0.253 no 4 −1.167 TCACCA 0.017%−0.146 no 4 0.899 TCACCC 0.012% NA no 4 0.396 TCACCG 0.011%  0.651 no 41.213 TCACGA 0.024% NA no 4 −1.241 TCACGC 0.013%  0.449 no 4 −0.583TCACGG 0.021%  0.253 no 4 −0.521 TCATAA 0.024% NA no 4 −2.852 TCATAC0.019% NA no 4 −2.260 TCATAG 0.018% −0.517 no 4 −1.141 TCATCA 0.022% NAno 4 −1.249 TCATCC 0.012%  0.274 no 4 −0.772 TCATCG 0.020%  0.752 no 4−1.097 TCATGA 0.024% NA no 4 −2.227 TCATGC 0.018% NA no 4 −0.559 TCATGG0.023% NA no 4 −0.187 TCCAAT 0.016% NA no 4 −1.686 TCCACT 0.012% NA no 4−2.259 TCCAGT 0.013% NA no 4 −0.435 TCCATA 0.011% NA no 4 −1.884 TCCATC0.013% NA no 4 −2.238 TCCATG 0.014% NA no 4 −0.464 TCCCCT 0.006% NA no 4−2.834 TCCCGT 0.010% NA no 4 −1.561 TCCCTA 0.010% −0.566 no 4 −1.649TCCCTC 0.007% NA no 4 −1.868 TCCCTG 0.011%  0.247 no 4 −1.229 TCCGAA0.018% NA no 4 −0.603 TCCGAC 0.013%  0.526 no 4 −0.994 TCCGAG 0.014% 0.308 no 4 0.708 TCCGCA 0.017% NA no 4 3.924 TCCGCC 0.006%  0.192 no 4−0.356 TCCGCG 0.014%  0.675 no 4 −0.386 TCCGGA 0.014%  0.636 no 4 0.382TCCGGC 0.008%  0.480 no 4 0.198 TCCGGG 0.011%  0.514 no 4 −0.296 TCCTAT0.008% −0.293 no 4 −1.800 TCCTCT 0.006% NA no 4 1.476 TCCTGT 0.008% NAno 4 −0.731 TCCTTA 0.008% −0.527 no 4 −1.399 TCCTTC 0.006% NA no 4−2.387 TCCTTG 0.009% NA no 4 −0.389 TCGAAT 0.023% NA no 4 −0.659 TCGACT0.016%  0.542 no 4 −0.567 TCGAGT 0.024% NA no 4 −0.308 TCGATA 0.017% NAno 4 −1.960 TCGATC 0.014%  0.582 no 4 −1.568 TCGATG 0.023%  0.337 no 40.044 TCGCAT 0.016% NA no 4 −0.904 TCGCCT 0.009%  0.492 no 4 −2.184TCGCGT 0.011%  0.436 no 4 −0.065 TCGCTA 0.016% NA no 4 −1.448 TCGCTC0.008%  0.356 no 4 −1.002 TCGCTG 0.013%  0.311 no 4 −1.082 TCGGAA 0.035% 0.447 no 4 −0.690 TCGGAC 0.018%  0.559 no 4 −0.018 TCGGAG 0.021%  0.315no 4 −0.928 TCGGCA 0.023% NA no 4 −0.004 TCGGCC 0.009%  0.441 no 4−0.727 TCGGCG 0.018%  0.863 no 4 −0.307 TCGGGA 0.025%  0.421 no 4 0.414TCGGGC 0.008%  0.350 no 4 3.317 TCGGGG 0.024%  0.237 no 4 0.171 TCGTAT0.011% NA no 4 −0.103 TCGTGT 0.015%  0.255 no 4 1.091 TCGTTA 0.018% NAno 4 −1.875 TCGTTC 0.010%  0.473 no 4 0.488 TCGTTG 0.017%  0.189 no 40.022 TCTAAT 0.016% −0.402 no 4 −1.638 TCTACT 0.012% NA no 4 −1.419TCTAGT 0.008% −0.450 no 4 −6.596 TCTATA 0.012% −0.491 no 4 −5.035 TCTATC0.008% NA no 4 −2.815 TCTATG 0.014% −0.240 no 4 −0.022 TCTCAT 0.009% NAno 4 −1.436 TCTCCT 0.007%  0.362 no 4 −2.722 TCTCGT 0.008% NA no 4 2.443TCTCTA 0.012% NA no 4 −2.895 TCTCTC 0.009% NA no 4 −1.950 TCTCTG 0.010% 0.164 no 4 −0.454 TCTGAA 0.025% NA no 4 −1.857 TCTGAC 0.014%  0.417 no4 −0.726 TCTGAG 0.019% NA no 4 −0.435 TCTGCA 0.013%  0.322 no 4 −6.092TCTGCC 0.011%  0.248 no 4 −2.157 TCTGCG 0.015%  0.698 no 4 −0.979 TCTGGA0.021% NA no 4 −0.788 TCTGGC 0.014% NA no 4 0.062 TCTGGG 0.020% NA no 4−0.821 TCTTAT 0.010% −0.317 no 4 −4.585 TCTTGT 0.008% NA no 4 −3.419TCTTTA 0.013% −0.477 no 4 −5.750 TCTTTC 0.011% NA no 4 −4.034 TCTTTG0.016% −0.218 no 4 −0.563 TGCAAA 0.037% −0.487 no 4 0.628 TGCAAC 0.021%NA no 4 −0.765 TGCAAG 0.033% NA no 4 −0.646 TGCACA 0.023% −0.335 no 4−0.123 TGCACC 0.012% NA no 4 1.585 TGCACG 0.025% NA no 4 −0.571 TGCAGA0.021% NA no 4 −2.629 TGCAGC 0.015% −0.365 no 4 −0.747 TGCAGG 0.020%−0.190 no 4 −0.828 TGCCAA 0.023% −0.257 no 4 −0.822 TGCCAC 0.014% −0.258no 4 0.707 TGCCAG 0.018% NA no 4 −0.233 TGCCCC 0.010% −0.255 no 4 1.354TGCCCG 0.013% NA no 4 0.875 TGCCGA 0.016% NA no 4 −0.401 TGCCGC 0.015%NA no 4 −0.379 TGCCGG 0.018%  0.357 no 4 −0.880 TGCTAA 0.030% −0.319 no4 0.980 TGCTAC 0.010% NA no 4 0.541 TGCTAG 0.021% −0.680 no 4 −1.668TGCTCA 0.013% −0.284 no 4 1.841 TGCTCC 0.007% NA no 4 0.367 TGCTCG0.013% NA no 4 −0.775 TGCTGA 0.017% NA no 4 −0.005 TGCTGC 0.009%  0.229no 4 −0.943 TGCTGG 0.017% −0.210 no 4 1.781 TGGAAA 0.037%  0.333 no 4−0.668 TGGAAC 0.022%  0.612 no 4 −0.753 TGGAAG 0.036%  0.395 no 4 −0.299TGGACA 0.029%  0.482 no 4 −0.524 TGGACC 0.014%  0.608 no 4 −1.530 TGGACG0.026%  0.686 no 4 −0.755 TGGAGA 0.041%  0.427 no 4 −1.040 TGGAGC 0.022% 0.299 no 4 −0.481 TGGAGG 0.034%  0.101 no 4 0.826 TGGCAA 0.029%  0.259no 4 −0.639 TGGCAC 0.022% −0.133 no 4 −0.046 TGGCAG 0.032% NA no 4−0.242 TGGCCA 0.018% NA no 4 −0.328 TGGCCC 0.012% NA no 4 0.218 TGGCCG0.011%  0.195 no 4 −0.952 TGGCGA 0.023%  0.443 no 4 −0.868 TGGCGC 0.008% 0.422 no 4 −0.003 TGGCGG 0.021%  0.301 no 4 0.063 TGGTAA 0.030% −0.538no 4 −0.010 TGGTAC 0.019% −0.144 no 4 0.413 TGGTAG 0.023% −0.626 no 4−0.138 TGGTCA 0.017% NA no 4 −0.950 TGGTCC 0.009%  0.136 no 4 −0.215TGGTCG 0.013%  0.156 no 4 1.450 TGGTGA 0.023% NA no 4 −0.493 TGGTGC0.018% NA no 4 −0.289 TGGTGG 0.025% −0.308 no 4 0.415 TGTAAA 0.043%−0.304 no 4 −0.358 TGTAAC 0.026% NA no 4 −0.018 TGTAAG 0.035% −0.362 no4 0.147 TGTACA 0.024% −0.205 no 4 −0.191 TGTACC 0.013% NA no 4 −0.029TGTACG 0.021%  0.188 no 4 −0.778 TGTAGA 0.037% −0.303 no 4 −1.079 TGTAGC0.020% −0.359 no 4 −0.526 TGTAGG 0.030% −0.688 no 4 −0.622 TGTCAA 0.027%NA no 4 0.482 TGTCAC 0.013% NA no 4 −0.717 TGTCAG 0.021% −0.433 no 40.164 TGTCCA 0.015% NA no 4 −0.235 TGTCCC 0.007% NA no 4 1.386 TGTCCG0.007%  0.234 no 4 0.057 TGTCGA 0.021%  0.362 no 4 −0.882 TGTCGC 0.014% 0.219 no 4 −0.680 TGTCGG 0.015%  0.312 no 4 −0.819 TGTTAA 0.028% −0.439no 4 −0.240 TGTTAC 0.016% NA no 4 0.656 TGTTAG 0.017% −0.758 no 4 −1.458TGTTCA 0.019% NA no 4 0.643 TGTTCG 0.013%  0.424 no 4 1.367 TGTTGA0.019% NA no 4 0.146 TGTTGC 0.012% NA no 4 0.101 TGTTGG 0.022% NA no 40.046 TTAAAA 0.041% −0.349 yes 4 −6.257 TTAAAC 0.019% NA yes 4 −5.625TTAAAG 0.037% −0.242 yes 4 −3.276 TTAACA 0.035% NA yes 4 −4.812 TTAACC0.023% NA yes 4 −4.758 TTAACG 0.029% NA yes 4 −3.931 TTAAGA 0.033%−0.217 yes 4 −7.483 TTAAGC 0.029% −0.260 yes 4 −5.977 TTAAGG 0.035%−0.489 yes 4 −5.448 TTACAA 0.027% NA no 4 −4.111 TTACAC 0.023% NA no 4−4.213 TTACAG 0.018% −0.207 no 4 −2.331 TTACCA 0.014% NA no 4 −4.483TTACCC 0.010% NA no 4 −2.309 TTACCG 0.011%  0.416 no 4 −1.287 TTACGA0.014%  0.307 no 4 −1.468 TTACGC 0.014%  0.331 no 4 −1.441 TTACGG 0.018%NA no 4 −1.053 TTATAA 0.029% −0.441 no 4 −4.000 TTATAC 0.019% NA no 4−5.871 TTATAG 0.026% −0.594 no 4 −3.787 TTATCA 0.026% NA no 4 −3.704TTATCC 0.008% NA no 4 −2.232 TTATCG 0.019%  0.238 no 4 −0.251 TTATGA0.026% NA no 4 −5.339 TTATGC 0.018% −0.300 no 4 −0.623 TTATGG 0.022%−0.263 no 4 −0.347 TTCAAT 0.018% NA no 4 −2.208 TTCACT 0.010% NA no 4−1.187 TTCAGT 0.019% −0.197 no 4 −0.135 TTCATA 0.016% NA no 4 −2.081TTCATC 0.015%  0.597 no 4 −0.541 TTCATG 0.016% NA no 4 −0.760 TTCCAT0.008% NA no 4 1.476 TTCCGT 0.007% NA no 4 −0.918 TTCCTC 0.006% NA no 4−0.978 TTCCTG 0.011%  0.388 no 4 −0.489 TTCGAA 0.022%  0.421 no 4 −0.274TTCGAC 0.013%  0.749 no 4 1.026 TTCGAG 0.015%  0.397 no 4 0.701 TTCGCA0.016%  0.460 no 4 −0.065 TTCGCC 0.010%  0.637 no 4 −0.549 TTCGCG 0.013% 0.720 no 4 −0.507 TTCGGA 0.017%  0.487 no 4 −0.120 TTCGGC 0.012%  0.615no 4 −0.684 TTCGGG 0.022%  0.326 no 4 −0.467 TTCTAT 0.009% −0.185 no 4−3.859 TTCTCT 0.010% NA no 4 0.032 TTCTGT 0.013% NA no 4 −0.825 TTCTTA0.012% −0.207 no 4 −4.174 TTCTTC 0.009%  0.446 no 4 −2.850 TTCTTG 0.012%−0.217 no 4 −0.295 TTGAAT 0.029% NA yes 4 −3.343 TTGACT 0.018% NA yes 4−3.981 TTGAGT 0.021% −0.224 yes 4 −3.268 TTGATA 0.026% −0.226 yes 4−3.154 TTGATC 0.014%  0.330 yes 4 −3.707 TTGATG 0.024% NA yes 4 −2.991TTGCAT 0.020% NA no 4 −1.414 TTGCCT 0.009%  0.262 no 4 0.493 TTGCGT0.014%  0.240 no 4 −1.217 TTGCTA 0.010% NA no 4 −0.981 TTGCTC 0.011%−0.151 no 4 −1.593 TTGCTG 0.010%  0.184 no 4 −1.199 TTGGAA 0.032%  0.206no 4 −0.962 TTGGAC 0.021%  0.315 no 4 0.463 TTGGAG 0.031% NA no 4 −0.221TTGGCA 0.021% NA no 4 −1.925 TTGGCC 0.008% NA no 4 −1.264 TTGGCG 0.018% 0.355 no 4 −0.284 TTGGGA 0.024% NA no 4 −2.123 TTGGGC 0.011% −0.138 no4 −2.203 TTGGGG 0.023% −0.218 no 4 −2.416 TTGTAT 0.017% NA no 4 −2.518TTGTCT 0.014% NA no 4 −2.588 TTGTGT 0.013% NA no 4 −2.719 TTGTTA 0.025%−0.337 no 4 −4.186 TTGTTC 0.011%  0.230 no 4 −3.284 TTGTTG 0.014% −0.150no 4 −1.180 TTTAAT 0.020% −0.494 no 4 −6.052 TTTACT 0.015% NA no 4−5.274 TTTAGT 0.018% −0.635 no 4 −9.622 TTTATA 0.019% −0.421 no 4 −5.136TTTATC 0.014% NA no 4 −5.023 TTTATG 0.015% −0.370 no 4 −1.536 TTTCAT0.014% NA no 4 −2.833 TTTCCT 0.008% NA no 4 −3.520 TTTCGT 0.013%  0.291no 4 −1.753 TTTCTA 0.019% NA no 4 −3.406 TTTCTC 0.014% NA no 4 −5.454TTTCTG 0.012% NA no 4 −3.087 TTTGAA 0.031% NA no 4 −2.719 TTTGAC 0.017%NA no 4 −2.842 TTTGAG 0.021% −0.225 no 4 0.059 TTTGCA 0.018% −0.243 no 4−3.287 TTTGCC 0.013% NA no 4 −1.957 TTTGCG 0.016%  0.274 no 4 1.190TTTGGA 0.031% NA no 4 −0.740 TTTGGC 0.018% NA no 4 −1.142 TTTGGG 0.021%−0.200 no 4 −2.438 TTTTAT 0.016% −0.433 no 4 −3.129 TTTTCT 0.012% NA no4 −5.242 TTTTGT 0.015% −0.281 no 4 −3.951 TTTTTA 0.017% −0.436 no 4−5.801 TTTTTC 0.009% NA no 4 −4.067 TTTTTG 0.015% −0.451 no 4 −4.376AAAAAA 0.116% NA no 5 −4.298 AAAAAC 0.083% NA no 5 −3.426 AAAAAG 0.096%NA no 5 −0.607 AAAACA 0.070% NA no 5 −2.840 AAAACC 0.036% NA no 5 −2.847AAAACG 0.066% NA no 5 −0.718 AAAAGA 0.099% NA no 5 −3.161 AAAAGC 0.070%NA no 5 −2.806 AAAAGG 0.101% −0.210 no 5 −2.186 AAACAA 0.076% NA no 5−2.675 AAACAC 0.040% NA no 5 −4.391 AAACAG 0.063% NA no 5 −1.710 AAACCA0.044% NA no 5 −1.597 AAACCC 0.023% −0.292 no 5 −2.155 AAACCG 0.040% 0.295 no 5 0.265 AAACGA 0.061%  0.408 no 5 −1.551 AAACGC 0.035%  0.399no 5 −1.063 AAACGG 0.056%  0.177 no 5 −0.487 AAATAA 0.064% NA no 5−4.264 AAATAC 0.038% NA no 5 −3.313 AAATAG 0.047% −0.518 no 5 −2.333AAATCA 0.044% NA no 5 −3.412 AAATCC 0.014% NA no 5 −3.685 AAATCG 0.035% 0.271 no 5 −0.576 AAATGA 0.058% NA no 5 −2.896 AAATGC 0.042% −0.223 no5 −2.509 AAATGG 0.055% NA no 5 −1.576 AACAAT 0.046% NA no 5 −1.641AACACT 0.031%  0.256 no 5 −1.171 AACAGT 0.044% NA no 5 −0.666 AACATA0.049% NA no 5 −1.138 AACATC 0.033%  0.351 no 5 −0.742 AACATG 0.042% NAno 5 −0.489 AACCAT 0.029% NA no 5 −0.757 AACCCT 0.018%  0.324 no 5−1.525 AACCGT 0.021% NA no 5 0.533 AACCTA 0.023% NA no 5 −0.741 AACCTC0.019%  0.286 no 5 −1.607 AACCTG 0.022%  0.458 no 5 0.184 AACGAA 0.059%NA no 5 −0.009 AACGAC 0.036%  0.481 no 5 −0.297 AACGAG 0.051% NA no 5−0.840 AACGCA 0.041% NA no 5 −1.264 AACGCC 0.022%  0.516 no 5 0.729AACGCG 0.042%  0.692 no 5 0.372 AACGGA 0.061%  0.780 no 5 −0.270 AACGGC0.034%  0.523 no 5 0.480 AACGGG 0.048%  0.288 no 5 −0.238 AACTAT 0.019%NA no 5 −1.804 AACTCT 0.017% NA no 5 −0.369 AACTGT 0.021% NA no 5 0.684AACTTA 0.024% NA no 5 −2.119 AACTTC 0.015%  0.414 no 5 −0.767 AACTTG0.032% NA no 5 0.526 AAGAAT 0.068%  0.613 no 5 −1.100 AAGACT 0.032% 0.778 no 5 −0.590 AAGAGT 0.058%  0.316 no 5 −1.370 AAGATA 0.063%  0.391no 5 −1.436 AAGATC 0.036%  0.637 no 5 −1.025 AAGATG 0.058%  0.465 no 5−0.342 AAGCAT 0.041% NA no 5 −1.973 AAGCCT 0.024% NA no 5 −1.669 AAGCGT0.027% NA no 5 −1.179 AAGCTA 0.035% NA no 5 −1.865 AAGCTC 0.020% NA no 5−0.488 AAGCTG 0.040%  0.235 no 5 0.107 AAGGAA 0.083%  0.545 no 5 −2.097AAGGAC 0.047%  0.571 no 5 −1.555 AAGGAG 0.058% NA no 5 −0.136 AAGGCA0.053% NA no 5 −2.465 AAGGCC 0.023% NA no 5 −1.155 AAGGCG 0.035%  0.306no 5 −0.214 AAGGGA 0.074% −0.207 no 5 −3.974 AAGGGC 0.038% −0.146 no 5−4.913 AAGGGG 0.069% −0.193 no 5 −2.523 AAGTAT 0.039% NA no 5 −2.379AAGTCT 0.024%  0.381 no 5 −1.489 AAGTGT 0.046% NA no 5 −1.648 AAGTTA0.043% NA no 5 −2.458 AAGTTC 0.026%  0.292 no 5 −3.454 AAGTTG 0.034% NAno 5 −1.179 AATAAT 0.040% −0.289 no 5 −3.529 AATACT 0.022% NA no 5−3.995 AATAGT 0.035% −0.463 no 5 −7.162 AATATA 0.042% −0.477 no 5 −3.683AATATC 0.021% NA no 5 −2.339 AATATG 0.040% −0.245 no 5 −0.688 AATCAT0.033% NA no 5 −2.366 AATCCT 0.018%  0.417 no 5 −1.551 AATCGT 0.027% 0.314 no 5 −1.588 AATCTA 0.024% NA no 5 −3.222 AATCTC 0.010% NA no 5−2.828 AATCTG 0.030%  0.228 no 5 −0.659 AATGAA 0.056% NA no 5 −2.047AATGAC 0.018%  0.349 no 5 −1.261 AATGAG 0.029% NA no 5 −0.549 AATGCA0.035% −0.225 no 5 −3.043 AATGCC 0.009% NA no 5 −1.035 AATGCG 0.025% 0.295 no 5 −0.655 AATGGA 0.043%  0.386 no 5 −0.864 AATGGC 0.024%  0.119no 5 −0.700 AATGGG 0.040% −0.266 no 5 −2.138 AATTAT 0.024% −0.392 no 5−4.140 AATTCT 0.006% NA no 5 −3.905 AATTGT 0.020% NA no 5 −3.972 AATTTA0.026% NA no 5 −3.956 AATTTC 0.013% NA no 5 −5.056 AATTTG 0.021% −0.175no 5 −2.374 ACAAAA 0.082% NA no 5 −2.854 ACAAAC 0.049% NA no 5 −2.644ACAAAG 0.070% NA no 5 −0.187 ACAACA 0.053% NA no 5 −1.154 ACAACC 0.027%NA no 5 −0.819 ACAACG 0.043%  0.587 no 5 0.377 ACAAGA 0.065%  0.488 no 5−0.926 ACAAGC 0.048%  0.353 no 5 −1.421 ACAAGG 0.065% NA no 5 −0.420ACACAA 0.048% NA no 5 −2.059 ACACAC 0.028% NA no 5 −3.690 ACACAG 0.048%NA no 5 −0.472 ACACCA 0.030% −0.127 no 5 −1.609 ACACCC 0.017% NA no 5−1.031 ACACCG 0.025%  0.536 no 5 −0.067 ACACGA 0.044% NA no 5 −0.517ACACGC 0.027%  0.497 no 5 −1.236 ACACGG 0.044%  0.350 no 5 −0.332 ACATAA0.047% NA no 5 −3.398 ACATAC 0.032% NA no 5 −3.445 ACATAG 0.045% −0.435no 5 −1.259 ACATCA 0.034% NA no 5 −2.158 ACATCC 0.015%  0.231 no 5−0.653 ACATCG 0.030%  0.571 no 5 −0.659 ACATGA 0.037% NA no 5 −2.797ACATGC 0.026% NA no 5 −0.300 ACATGG 0.049% NA no 5 −0.971 ACCAAT 0.029%NA no 5 0.074 ACCACT 0.015% NA no 5 −0.829 ACCAGT 0.030% NA no 5 −0.548ACCATA 0.028% −0.569 no 5 −1.492 ACCATC 0.017% NA no 5 0.452 ACCATG0.029% NA no 5 −0.179 ACCCAT 0.019% −0.188 no 5 −0.502 ACCCCT 0.013%−0.152 no 5 −1.971 ACCCGT 0.016%  0.279 no 5 −0.472 ACCCTA 0.012% −0.298no 5 −3.091 ACCCTC 0.010%  0.137 no 5 −1.155 ACCCTG 0.016%  0.155 no 50.953 ACCGAA 0.035% NA no 5 −0.100 ACCGAC 0.025% NA no 5 0.296 ACCGAG0.032% NA no 5 0.018 ACCGCA 0.021% NA no 5 −0.489 ACCGCC 0.017% NA no 51.759 ACCGCG 0.022%  0.487 no 5 −0.743 ACCGGA 0.034% NA no 5 −0.278ACCGGC 0.019% NA no 5 0.949 ACCGGG 0.030%  0.550 no 5 −0.455 ACCTAT0.016% −0.268 no 5 −1.735 ACCTCT 0.012% NA no 5 −1.503 ACCTGT 0.020% NAno 5 0.204 ACCTTA 0.021% NA no 5 −1.504 ACCTTC 0.012% NA no 5 −1.703ACCTTG 0.016% NA no 5 −0.361 ACGAAT 0.047% NA no 5 −0.211 ACGACT 0.021% 0.496 no 5 −0.097 ACGAGT 0.037% NA no 5 −0.119 ACGATA 0.033% NA no 5−0.708 ACGATC 0.025%  0.631 no 5 −0.942 ACGATG 0.035%  0.361 no 5 0.446ACGCAT 0.025% NA no 5 −1.115 ACGCCT 0.020%  0.525 no 5 −0.441 ACGCGT0.022%  0.363 no 5 −0.420 ACGCTA 0.023% NA no 5 −0.307 ACGCTC 0.017% 0.387 no 5 0.271 ACGCTG 0.023%  0.380 no 5 −0.317 ACGGAA 0.061%  0.504no 5 −0.653 ACGGAC 0.036%  0.676 no 5 −0.672 ACGGAG 0.041%  0.381 no 5−0.388 ACGGCA 0.031% NA no 5 −0.083 ACGGCC 0.021%  0.363 no 5 0.717ACGGCG 0.024%  0.709 no 5 0.796 ACGGGA 0.044%  0.425 no 5 0.084 ACGGGC0.035%  0.359 no 5 0.315 ACGGGG 0.043%  0.204 no 5 −0.443 ACGTAT 0.030%NA no 5 −1.543 ACGTCT 0.021%  0.513 no 5 −0.717 ACGTGT 0.028% NA no 5−0.255 ACGTTA 0.033% NA no 5 −1.795 ACGTTC 0.018%  0.520 no 5 −0.743ACGTTG 0.032%  0.252 no 5 −0.021 ACTAAT 0.033% −0.334 no 5 −3.642 ACTACT0.016%  0.308 no 5 −2.192 ACTAGT 0.025% −0.409 no 5 −7.390 ACTATA 0.024%−0.391 no 5 −4.008 ACTATC 0.021% NA no 5 −3.883 ACTATG 0.021% NA no 5−0.814 ACTCAT 0.023% NA no 5 −3.471 ACTCCT 0.017%  0.416 no 5 −2.373ACTCGT 0.018%  0.266 no 5 −1.264 ACTCTA 0.022% −0.394 no 5 −3.332 ACTCTC0.014% NA no 5 −2.268 ACTCTG 0.021%  0.194 no 5 −0.477 ACTGAA 0.040% NAno 5 −0.118 ACTGAC 0.023%  0.335 no 5 −1.737 ACTGAG 0.025% NA no 5 0.822ACTGCA 0.025%  0.203 no 5 −2.160 ACTGCC 0.018% NA no 5 0.120 ACTGCG0.024%  0.510 no 5 0.118 ACTGGA 0.037% NA no 5 −0.286 ACTGGC 0.025% NAno 5 −0.588 ACTGGG 0.037% NA no 5 −1.048 ACTTAT 0.023% NA no 5 −3.348ACTTCT 0.012%  0.263 no 5 −2.599 ACTTGT 0.018% NA no 5 −2.260 ACTTTA0.025% −0.551 no 5 −6.474 ACTTTC 0.012% NA no 5 −2.527 ACTTTG 0.018%−0.155 no 5 −0.536 AGCAAA 0.066% NA no 5 −0.231 AGCAAC 0.040% NA no 5−0.478 AGCAAG 0.052% NA no 5 −0.850 AGCACA 0.035% NA no 5 −0.568 AGCACC0.020% −0.302 no 5 −1.046 AGCACG 0.038% NA no 5 −0.230 AGCAGA 0.048% NAno 5 −0.701 AGCAGC 0.027% −0.295 no 5 0.466 AGCAGG 0.039% −0.304 no 5−0.610 AGCCAA 0.033% NA no 5 0.048 AGCCAC 0.021% NA no 5 −0.708 AGCCAG0.035% −0.193 no 5 −0.625 AGCCCA 0.024% −0.292 no 5 −1.079 AGCCCC 0.018%−0.233 no 5 0.248 AGCCCG 0.022% NA no 5 0.030 AGCCGA 0.031% NA no 50.240 AGCCGC 0.018% NA no 5 −0.319 AGCCGG 0.029%  0.257 no 5 −0.016AGCTAA 0.033% −0.436 no 5 −0.386 AGCTAC 0.025% NA no 5 −0.221 AGCTAG0.041% −0.772 no 5 −0.344 AGCTCA 0.034% NA no 5 −0.220 AGCTCC 0.018% NAno 5 −0.968 AGCTCG 0.023% NA no 5 1.106 AGCTGA 0.032% NA no 5 −0.143AGCTGC 0.017%  0.152 no 5 −0.427 AGCTGG 0.029% −0.227 no 5 −0.206 AGGAAA0.092% NA no 5 −3.561 AGGAAC 0.064%  0.338 no 5 −2.293 AGGAAG 0.066% NAno 5 −1.064 AGGACA 0.066% NA no 5 −3.251 AGGACC 0.034%  0.246 no 5−1.549 AGGACG 0.047%  0.394 no 5 −0.096 AGGAGA 0.078% NA no 5 −1.908AGGAGC 0.040%  0.336 no 5 −1.938 AGGAGG 0.065% −0.147 no 5 −1.028 AGGCAA0.055% NA no 5 −2.114 AGGCAC 0.039% NA no 5 −3.296 AGGCAG 0.052% −0.490no 5 −1.343 AGGCCA 0.035% NA no 5 −1.280 AGGCCC 0.029% NA no 5 −0.420AGGCCG 0.031% NA no 5 −0.324 AGGCGA 0.040% NA no 5 −0.846 AGGCGC 0.025%NA no 5 1.091 AGGCGG 0.035% NA no 5 −0.488 AGGTAA 0.065% −0.555 no 5−5.154 AGGTAC 0.038% NA no 5 −4.296 AGGTAG 0.042% −0.871 no 5 −3.122AGGTCA 0.043% NA no 5 −2.539 AGGTCC 0.025% −0.226 no 5 −1.406 AGGTCG0.032% NA no 5 −0.550 AGGTGA 0.039% −0.429 no 5 −2.689 AGGTGC 0.033%−0.262 no 5 −1.279 AGGTGG 0.044% −0.423 no 5 −0.072 AGTAAA 0.063% NA no5 −1.632 AGTAAC 0.050% NA no 5 −0.695 AGTAAG 0.062% −0.505 no 5 −0.778AGTACA 0.044% NA no 5 −1.271 AGTACC 0.029% NA no 5 −1.082 AGTACG 0.046%NA no 5 0.024 AGTAGA 0.052% NA no 5 −3.087 AGTAGC 0.032% −0.483 no 5−2.096 AGTAGG 0.052% −0.703 no 5 −2.394 AGTCAA 0.049% NA no 5 −0.576AGTCAC 0.024% NA no 5 −0.941 AGTCAG 0.039% −0.684 no 5 −1.114 AGTCCA0.024% NA no 5 −0.521 AGTCCC 0.015% −0.237 no 5 −0.021 AGTCCG 0.018% 0.277 no 5 0.367 AGTCGA 0.034% NA no 5 0.016 AGTCGC 0.023%  0.365 no 5−0.564 AGTCGG 0.031%  0.160 no 5 −0.096 AGTTAA 0.054% −0.172 no 5 −1.972AGTTAC 0.020%  0.192 no 5 −0.533 AGTTAG 0.040% −0.645 no 5 −0.840 AGTTCA0.031%  0.204 no 5 −1.079 AGTTCC 0.013% −0.098 no 5 1.774 AGTTCG 0.021% 0.505 no 5 2.317 AGTTGA 0.039%  0.119 no 5 0.377 AGTTGC 0.021%  0.176no 5 1.008 AGTTGG 0.034% NA no 5 −0.493 ATAAAA 0.080% −0.542 yes 5−5.299 ATAAAC 0.059% NA yes 5 −4.890 ATAAAG 0.058% −0.271 yes 5 −3.286ATAACA 0.058% −0.364 yes 5 −6.056 ATAACC 0.031% −0.274 yes 5 −3.913ATAACG 0.047% NA yes 5 −3.211 ATAAGA 0.056% NA yes 5 −5.331 ATAAGC0.040% NA yes 5 −5.799 ATAAGG 0.061% −0.365 yes 5 −5.184 ATACAA 0.047%NA no 5 −2.992 ATACAC 0.032% NA no 5 −3.030 ATACAG 0.040% NA no 5 −1.862ATACCA 0.029% NA no 5 −1.355 ATACCC 0.017% −0.229 no 5 −1.258 ATACCG0.019%  0.319 no 5 −0.173 ATACGA 0.043% NA no 5 −2.295 ATACGC 0.022% 0.358 no 5 −1.628 ATACGG 0.038%  0.193 no 5 −0.746 ATATAA 0.056% −0.361no 5 −5.270 ATATAC 0.037% NA no 5 −4.232 ATATAG 0.041% −0.674 no 5−2.537 ATATCA 0.036% NA no 5 −4.023 ATATCC 0.016% NA no 5 −0.528 ATATCG0.032% NA no 5 0.356 ATATGA 0.043% NA no 5 −1.698 ATATGC 0.030% −0.243no 5 −2.881 ATATGG 0.043% NA no 5 −0.719 ATCAAT 0.036% NA no 5 −0.510ATCACT 0.021% NA no 5 0.192 ATCAGT 0.029% −0.409 no 5 −1.810 ATCATA0.034% NA no 5 −0.557 ATCATC 0.021% NA no 5 0.534 ATCATG 0.028% NA no 5−0.848 ATCCAT 0.026% NA no 5 −0.850 ATCCCT 0.014% NA no 5 −1.684 ATCCGT0.015% NA no 5 −1.359 ATCCTA 0.017% NA no 5 −0.827 ATCCTC 0.014% NA no 5−0.712 ATCCTG 0.016%  0.447 no 5 0.126 ATCGAA 0.041% NA no 5 −0.076ATCGAC 0.020%  0.539 no 5 −0.078 ATCGAG 0.037% NA no 5 −0.805 ATCGCA0.030% NA no 5 0.443 ATCGCC 0.022%  0.290 no 5 0.958 ATCGCG 0.025% 0.541 no 5 −0.167 ATCGGA 0.039%  0.342 no 5 −0.115 ATCGGC 0.025%  0.334no 5 0.218 ATCGGG 0.035%  0.390 no 5 −0.354 ATCTAT 0.021% −0.315 no 5−0.895 ATCTCT 0.015% NA no 5 −1.080 ATCTGT 0.023% NA no 5 0.256 ATCTTA0.022% −0.350 no 5 −0.819 ATCTTC 0.016% NA no 5 −1.648 ATCTTG 0.017%−0.191 no 5 −0.218 ATGAAT 0.047%  0.279 yes 5 −3.010 ATGACT 0.032% 0.367 yes 5 −1.853 ATGAGT 0.043% NA yes 5 −4.072 ATGATA 0.041% NA yes 5−5.173 ATGATC 0.029%  0.442 yes 5 −4.543 ATGATG 0.035%  0.187 yes 5−2.675 ATGCAT 0.031% NA no 5 −2.752 ATGCCT 0.012%  0.331 no 5 0.031ATGCGT 0.024% NA no 5 −1.629 ATGCTA 0.030% NA no 5 −2.856 ATGCTC 0.020%NA no 5 −4.102 ATGCTG 0.021%  0.208 no 5 0.015 ATGGAA 0.052%  0.393 no 5−0.996 ATGGAC 0.039%  0.589 no 5 −0.534 ATGGAG 0.047%  0.229 no 5 −0.418ATGGCA 0.044% NA no 5 −1.948 ATGGCC 0.022% NA no 5 0.689 ATGGCG 0.034% 0.388 no 5 −0.119 ATGGGA 0.064%  0.054 no 5 −2.200 ATGGGC 0.028% −0.106no 5 −2.348 ATGGGG 0.052% −0.331 no 5 −2.867 ATGTAT 0.034% NA no 5−3.231 ATGTCT 0.019% NA no 5 −3.313 ATGTGT 0.030% NA no 5 −2.322 ATGTTA0.041% NA no 5 −3.521 ATGTTC 0.024%  0.354 no 5 −4.463 ATGTTG 0.030% NAno 5 −1.595 ATTAAT 0.042% −0.360 no 5 −4.518 ATTACT 0.016% NA no 5−1.163 ATTAGT 0.034% −0.437 no 5 −9.337 ATTATA 0.038% −0.813 no 5 −4.559ATTATC 0.025% NA no 5 −5.888 ATTATG 0.030% −0.355 no 5 −2.309 ATTCAT0.019% NA no 5 −1.547 ATTCCT 0.007% NA no 5 −0.611 ATTCGT 0.017% NA no 51.588 ATTCTA 0.020% NA no 5 −3.930 ATTCTC 0.015% NA no 5 −2.827 ATTCTG0.020%  0.188 no 5 −1.028 ATTGAA 0.049% NA no 5 −2.491 ATTGAC 0.029% NAno 5 −2.342 ATTGAG 0.034% NA no 5 −0.692 ATTGCA 0.027% −0.178 no 5−3.833 ATTGCC 0.015% NA no 5 −2.134 ATTGCG 0.026%  0.287 no 5 −0.600ATTGGA 0.042%  0.347 no 5 −0.875 ATTGGC 0.028% NA no 5 −1.255 ATTGGG0.040% −0.103 no 5 −2.010 ATTTAT 0.023% −0.260 no 5 −3.982 ATTTCT 0.017%NA no 5 −6.887 ATTTGT 0.023% NA no 5 −4.055 ATTTTA 0.027% −0.725 no 5−5.043 ATTTTC 0.017% NA no 5 −3.757 ATTTTG 0.029% −0.257 no 5 −2.146CAAAAA 0.047% −0.255 no 5 −2.163 CAAAAC 0.042% NA no 5 −2.136 CAAAAG0.037% NA no 5 −0.198 CAAACA 0.040% NA no 5 −1.402 CAAACC 0.025% NA no 5−1.664 CAAACG 0.035%  0.292 no 5 0.022 CAAAGA 0.034%  0.230 no 5 −0.798CAAAGC 0.025% NA no 5 −1.331 CAAAGG 0.043% NA no 5 −0.013 CAACAA 0.035% 0.269 no 5 −0.491 CAACAC 0.019%  0.282 no 5 −1.086 CAACAG 0.026% NA no5 −0.336 CAACCA 0.021% NA no 5 −0.273 CAACCC 0.012% NA no 5 −0.916CAACCG 0.021% NA no 5 −0.342 CAACGA 0.027%  0.224 no 5 −0.189 CAACGC0.020%  0.542 no 5 −0.395 CAACGG 0.031%  0.503 no 5 −0.182 CAATAA 0.032%−0.286 no 5 −2.882 CAATAC 0.018% NA no 5 −0.569 CAATAG 0.029% −0.465 no5 −1.951 CAATCA 0.026% NA no 5 −1.283 CAATCC 0.014% NA no 5 0.622 CAATCG0.020%  0.297 no 5 −0.238 CAATGA 0.024%  0.266 no 5 −1.142 CAATGC 0.017%NA no 5 −0.317 CAATGG 0.028% NA no 5 −0.403 CACAAT 0.029% −0.217 no 5−0.731 CACACT 0.017% NA no 5 −1.344 CACAGT 0.019% −0.197 no 5 −1.502CACATA 0.023% −0.538 no 5 −1.630 CACATC 0.012% NA no 5 0.617 CACATG0.019% NA no 5 0.305 CACCAT 0.016% −0.373 no 5 −0.703 CACCCT 0.012% NAno 5 −3.190 CACCGT 0.012% NA no 5 0.124 CACCTA 0.015% −0.737 no 5 0.587CACCTC 0.011% NA no 5 −1.006 CACCTG 0.010%  0.154 no 5 −0.859 CACGAA0.034% NA no 5 −1.082 CACGAC 0.016% NA no 5 0.161 CACGAG 0.027% NA no 50.053 CACGCA 0.017% NA no 5 0.202 CACGCC 0.014%  0.268 no 5 −0.845CACGCG 0.020%  0.289 no 5 −0.662 CACGGA 0.021%  0.304 no 5 −0.142 CACGGC0.019% NA no 5 −0.459 CACGGG 0.024%  0.344 no 5 0.662 CACTAT 0.013%−0.324 no 5 −1.230 CACTCT 0.016% −0.268 no 5 −2.049 CACTGT 0.011% NA no5 −1.174 CACTTA 0.015% −0.562 no 5 −1.130 CACTTC 0.011% NA no 5 −1.667CACTTG 0.015% −0.275 no 5 −1.849 CAGAAT 0.029%  0.207 no 5 −1.732 CAGACT0.027% NA no 5 −1.070 CAGAGT 0.031% NA no 5 −0.940 CAGATA 0.032% −0.309no 5 −1.291 CAGATC 0.014% NA no 5 −0.205 CAGATG 0.031%  0.190 no 5 0.162CAGCAT 0.025% −0.194 no 5 0.369 CAGCCT 0.016% −0.303 no 5 −0.481 CAGCGT0.015% NA no 5 0.330 CAGCTA 0.018% −0.349 no 5 −1.378 CAGCTC 0.010% NAno 5 −0.268 CAGCTG 0.015% NA no 5 0.199 CAGGAA 0.039% NA no 5 −0.800CAGGAC 0.025%  0.250 no 5 −0.298 CAGGAG 0.033% NA no 5 0.020 CAGGCA0.029% −0.223 no 5 −3.182 CAGGCC 0.019% NA no 5 −0.707 CAGGCG 0.023% NAno 5 −0.949 CAGGGA 0.045% −0.328 no 5 −4.328 CAGGGC 0.016% −0.181 no 5−3.990 CAGGGG 0.033% −0.227 no 5 −2.819 CAGTAT 0.024% −0.363 no 5 −0.732CAGTCT 0.013% NA no 5 −1.272 CAGTGT 0.020% −0.196 no 5 −0.107 CAGTTA0.023% −0.341 no 5 −1.461 CAGTTC 0.011% NA no 5 −1.817 CAGTTG 0.016% NAno 5 −0.664 CATAAT 0.025% −0.348 no 5 −1.706 CATACT 0.012% NA no 5−2.389 CATAGT 0.016% −0.342 no 5 −4.310 CATATA 0.015% −0.414 no 5 −1.444CATATC 0.013% NA no 5 −1.787 CATATG 0.020% −0.169 no 5 0.027 CATCAT0.019% NA no 5 −0.887 CATCCT 0.008% NA no 5 −0.945 CATCGT 0.014% NA no 50.552 CATCTA 0.016% −0.335 no 5 −0.187 CATCTC 0.009% NA no 5 −0.670CATCTG 0.020%  0.215 no 5 0.405 CATGAA 0.033%  0.373 no 5 −1.218 CATGAC0.009%  0.274 no 5 0.391 CATGAG 0.016% NA no 5 0.562 CATGCA 0.026%−0.095 no 5 −1.129 CATGCC 0.009% NA no 5 0.172 CATGCG 0.020% NA no 5−0.372 CATGGA 0.027%  0.524 no 5 0.007 CATGGC 0.016% NA no 5 −0.052CATGGG 0.026%  0.101 no 5 −0.444 CATTAT 0.015% −0.435 no 5 −4.230 CATTCT0.009% NA no 5 −1.799 CATTGT 0.011% NA no 5 −2.348 CATTTA 0.014% −0.404no 5 −1.953 CATTTC 0.008% NA no 5 −3.017 CATTTG 0.017% −0.160 no 5−2.055 CCAAAA 0.027% −0.592 no 5 −2.109 CCAAAC 0.022% −0.360 no 5 −1.518CCAAAG 0.025% −0.218 no 5 −0.565 CCAACA 0.019% NA no 5 −0.150 CCAACC0.011% NA no 5 −0.488 CCAACG 0.020%  0.408 no 5 0.002 CCAAGA 0.019% NAno 5 −0.890 CCAAGC 0.016% NA no 5 −0.437 CCAAGG 0.022% NA no 5 −0.256CCACAA 0.027% NA no 5 −1.804 CCACAC 0.015% NA no 5 −1.872 CCACAG 0.015%−0.283 no 5 −0.639 CCACCA 0.014% −0.597 no 5 −1.636 CCACCC 0.010% −0.303no 5 1.119 CCACCG 0.012% NA no 5 −0.229 CCACGA 0.018%  0.317 no 5 −0.224CCACGC 0.011% NA no 5 −0.187 CCACGG 0.018%  0.426 no 5 −0.510 CCATAA0.018% −0.566 no 5 −2.321 CCATAC 0.013% −0.342 no 5 −1.822 CCATAG 0.015%−0.497 no 5 −1.244 CCATCA 0.014% −0.216 no 5 −1.072 CCATCC 0.009% NA no5 0.526 CCATCG 0.013%  0.391 no 5 −0.053 CCATGA 0.014% NA no 5 −0.894CCATGC 0.011% NA no 5 −0.891 CCATGG 0.014%  0.183 no 5 −1.268 CCCAAT0.014% −0.365 no 5 −1.469 CCCACT 0.011% −0.255 no 5 −1.277 CCCAGT 0.010%−0.388 no 5 −2.238 CCCATA 0.012% −0.475 no 5 −3.772 CCCATC 0.010% NA no5 −1.096 CCCATG 0.012% NA no 5 0.331 CCCCCT 0.006% −0.217 no 5 −3.983CCCCGT 0.010% NA no 5 −1.571 CCCCTA 0.007% −0.434 no 5 −4.929 CCCCTG0.007%  0.114 no 5 0.211 CCCGAA 0.015%  0.281 no 5 −0.873 CCCGAC 0.014% 0.264 no 5 0.265 CCCGAG 0.016%  0.320 no 5 0.805 CCCGCA 0.014% NA no 5−1.168 CCCGCC 0.008% NA no 5 0.112 CCCGCG 0.008%  0.571 no 5 −0.368CCCGGA 0.013%  0.454 no 5 0.068 CCCGGC 0.010% NA no 5 −0.045 CCCGGG0.010%  0.386 no 5 0.233 CCCTAT 0.006% −0.386 no 5 −4.151 CCCTCT 0.006%NA no 5 −0.306 CCCTGT 0.007% NA no 5 −0.619 CCCTTA 0.013% −0.622 no 5−5.544 CCCTTC 0.006% NA no 5 0.005 CCCTTG 0.006% −0.092 no 5 −1.191CCGAAT 0.017% NA no 5 −0.405 CCGACT 0.009% NA no 5 −0.619 CCGAGT 0.018% 0.211 no 5 −0.240 CCGATA 0.016% NA no 5 −0.167 CCGATC 0.008% NA no 50.961 CCGATG 0.018%  0.275 no 5 0.722 CCGCAT 0.014% NA no 5 −0.323CCGCCT 0.010% NA no 5 −0.453 CCGCGT 0.007%  0.411 no 5 0.802 CCGCTA0.017% NA no 5 −0.641 CCGCTC 0.008%  0.224 no 5 −1.731 CCGCTG 0.006% 0.337 no 5 1.427 CCGGAA 0.028%  0.524 no 5 0.192 CCGGAC 0.012%  0.288no 5 −0.652 CCGGAG 0.020%  0.622 no 5 −0.362 CCGGCA 0.017% −0.276 no 51.306 CCGGCC 0.010% NA no 5 0.175 CCGGCG 0.017%  0.621 no 5 −1.036CCGGGA 0.020%  0.590 no 5 0.206 CCGGGC 0.012%  0.454 no 5 −0.736 CCGGGG0.019%  0.358 no 5 −0.436 CCGTAT 0.009% NA no 5 0.872 CCGTCT 0.006% 0.337 no 5 −0.172 CCGTTA 0.013% −0.283 no 5 −3.315 CCGTTC 0.009%  0.196no 5 0.261 CCGTTG 0.010%  0.241 no 5 −0.661 CCTAAT 0.010% −0.628 no 5−3.190 CCTACT 0.008% NA no 5 0.297 CCTAGT 0.006% −0.517 no 5 −5.949CCTATA 0.010% −0.599 no 5 −2.207 CCTATC 0.007% −0.285 no 5 −6.011 CCTATG0.008% −0.201 no 5 −1.218 CCTCAT 0.009% NA no 5 −0.277 CCTCCT 0.006% NAno 5 −1.459 CCTCGT 0.009%  0.284 no 5 −0.414 CCTCTA 0.011% −0.215 no 5−2.105 CCTCTC 0.005% NA no 5 1.159 CCTCTG 0.008%  0.206 no 5 0.809CCTGAA 0.021% NA no 5 −0.274 CCTGAC 0.010% NA no 5 −0.072 CCTGAG 0.011%NA no 5 0.683 CCTGCA 0.013%  0.332 no 5 −1.474 CCTGCC 0.007%  0.151 no 5−0.210 CCTGCG 0.015%  0.584 no 5 1.012 CCTGGA 0.011%  0.407 no 5 0.176CCTGGC 0.012% NA no 5 −0.365 CCTGGG 0.013%  0.277 no 5 0.803 CCTTAT0.007% −0.537 no 5 −1.326 CCTTCT 0.005% NA no 5 −2.992 CCTTGT 0.009%−0.207 no 5 −1.603 CCTTTA 0.005% −0.881 no 5 −4.138 CCTTTG 0.006% −0.241no 5 −1.149 CGCAAA 0.026% NA no 5 0.561 CGCAAC 0.021%  0.386 no 5 0.278CGCAAG 0.020% NA no 5 0.669 CGCACA 0.020% NA no 5 −2.160 CGCACC 0.009% 0.280 no 5 1.388 CGCACG 0.013%  0.604 no 5 0.400 CGCAGA 0.023% NA no 5−0.597 CGCAGC 0.012% −0.402 no 5 −0.575 CGCAGG 0.022% NA no 5 0.050CGCCAA 0.014% NA no 5 0.443 CGCCAC 0.011% NA no 5 0.179 CGCCAG 0.010% 0.298 no 5 −1.002 CGCCCA 0.007%  0.225 no 5 −0.574 CGCCCC 0.008% NA no5 −1.953 CGCCCG 0.005%  0.636 no 5 0.220 CGCCGA 0.009%  0.450 no 5−1.108 CGCCGC 0.006%  0.353 no 5 2.704 CGCCGG 0.010%  0.746 no 5 0.998CGCTAA 0.014% NA no 5 0.149 CGCTAC 0.008%  0.302 no 5 0.629 CGCTAG0.012% −0.399 no 5 −0.124 CGCTCA 0.009% NA no 5 0.549 CGCTCC 0.008% 0.260 no 5 0.173 CGCTCG 0.009%  0.487 no 5 −0.835 CGCTGA 0.013%  0.545no 5 −1.332 CGCTGC 0.009%  0.418 no 5 −1.093 CGCTGG 0.011% NA no 5−0.925 CGGAAA 0.035% NA no 5 0.338 CGGAAC 0.023%  0.618 no 5 0.258CGGAAG 0.026%  0.528 no 5 0.224 CGGACA 0.026% NA no 5 −0.284 CGGACC0.016%  0.447 no 5 0.568 CGGACG 0.026%  0.841 no 5 0.639 CGGAGA 0.026% 0.599 no 5 −1.101 CGGAGC 0.017%  0.618 no 5 0.538 CGGAGG 0.029%  0.385no 5 −0.032 CGGCAA 0.025% NA no 5 −0.210 CGGCAC 0.015% NA no 5 0.170CGGCAG 0.021% NA no 5 0.374 CGGCCA 0.012%  0.142 no 5 −0.568 CGGCCC0.011% NA no 5 0.288 CGGCCG 0.009%  0.460 no 5 2.910 CGGCGA 0.018% 0.686 no 5 1.084 CGGCGC 0.009%  0.595 no 5 −0.606 CGGCGG 0.018%  0.721no 5 −0.511 CGGTAA 0.024% NA no 5 −0.222 CGGTAC 0.015%  0.364 no 5 0.310CGGTAG 0.015% −0.530 no 5 −0.516 CGGTCA 0.014% NA no 5 −0.746 CGGTCC0.007%  0.431 no 5 −0.815 CGGTCG 0.013%  0.483 no 5 0.514 CGGTGA 0.018%NA no 5 0.579 CGGTGC 0.011% NA no 5 −0.800 CGGTGG 0.015% NA no 5 1.378CGTAAA 0.026% NA no 5 0.878 CGTAAC 0.016% NA no 5 0.417 CGTAAG 0.018% NAno 5 0.358 CGTACA 0.016% NA no 5 0.019 CGTACC 0.010%  0.277 no 5 0.658CGTACG 0.016%  0.408 no 5 1.020 CGTAGA 0.020% NA no 5 −0.415 CGTAGC0.011% −0.294 no 5 0.979 CGTAGG 0.015% −0.484 no 5 −0.882 CGTCAA 0.019% 0.515 no 5 0.678 CGTCAC 0.011%  0.401 no 5 0.156 CGTCAG 0.014% NA no 50.073 CGTCCA 0.008%  0.640 no 5 0.170 CGTCCC 0.007%  0.218 no 5 0.041CGTCCG 0.010%  0.753 no 5 −0.220 CGTCGA 0.015%  0.885 no 5 0.287 CGTCGC0.010%  0.885 no 5 −0.034 CGTCGG 0.006%  0.844 no 5 −0.670 CGTTAA 0.021%NA no 5 0.155 CGTTAC 0.009% NA no 5 −1.673 CGTTAG 0.012% −0.626 no 5−2.079 CGTTCA 0.012% NA no 5 0.168 CGTTCC 0.006%  0.395 no 5 1.633CGTTCG 0.010%  0.601 no 5 0.885 CGTTGA 0.013% NA no 5 −1.480 CGTTGC0.010%  0.191 no 5 −0.171 CGTTGG 0.012%  0.290 no 5 −0.722 CTAAAA 0.020%−0.424 yes 5 −5.083 CTAAAC 0.012% −0.456 yes 5 −3.039 CTAAAG 0.020%−0.364 yes 5 −3.512 CTAACA 0.013% NA yes 5 −4.892 CTAACC 0.007% −0.217yes 5 −2.610 CTAACG 0.008% NA yes 5 −2.195 CTAAGA 0.019% NA yes 5 −4.433CTAAGC 0.012% −0.283 yes 5 −4.345 CTAAGG 0.018% −0.377 yes 5 −4.084CTACAA 0.013% NA no 5 0.791 CTACAC 0.007% NA no 5 −0.163 CTACAG 0.012%NA no 5 −0.758 CTACCA 0.006% −0.188 no 5 0.181 CTACCC 0.004% −0.211 no 5−0.343 CTACCG 0.010%  0.356 no 5 −0.436 CTACGA 0.012%  0.366 no 5 −0.213CTACGC 0.006%  0.446 no 5 0.518 CTACGG 0.010%  0.503 no 5 0.285 CTATAA0.019% −0.566 no 5 −3.209 CTATAC 0.006% NA no 5 −2.641 CTATAG 0.015%−0.604 no 5 −0.860 CTATCA 0.009% −0.456 no 5 −4.031 CTATCC 0.005% NA no5 −5.014 CTATCG 0.010% NA no 5 0.587 CTATGA 0.011% NA no 5 −2.579 CTATGC0.006% −0.228 no 5 −1.462 CTATGG 0.011% NA no 5 −1.357 CTCAAT 0.016% NAno 5 −2.638 CTCACT 0.007% NA no 5 −3.336 CTCAGT 0.014% NA no 5 −2.816CTCATA 0.011% −0.431 no 5 −1.054 CTCATC 0.011% NA no 5 −0.961 CTCATG0.010% NA no 5 0.531 CTCCAT 0.009% NA no 5 0.155 CTCCGT 0.007%  0.481 no5 −1.212 CTCCTA 0.005% NA no 5 −3.446 CTCCTC 0.005% NA no 5 −1.099CTCCTG 0.007%  0.444 no 5 0.418 CTCGAA 0.015% NA no 5 −0.108 CTCGAC0.010%  0.491 no 5 −1.782 CTCGAG 0.012%  0.308 no 5 1.826 CTCGCA 0.008%NA no 5 −1.403 CTCGCG 0.015%  0.536 no 5 −0.761 CTCGGA 0.013%  0.520 no5 0.278 CTCGGC 0.009%  0.432 no 5 1.334 CTCGGG 0.012%  0.323 no 5 1.920CTCTAT 0.009% −0.374 no 5 −4.034 CTCTCT 0.007% NA no 5 −0.997 CTCTGT0.006% NA no 5 −3.627 CTCTTA 0.012% −0.642 no 5 −2.883 CTCTTC 0.004% NAno 5 0.471 CTCTTG 0.008% −0.257 no 5 −0.439 CTGAAT 0.023% NA yes 5−1.424 CTGACT 0.012% NA yes 5 −2.077 CTGAGT 0.015% NA yes 5 −3.901CTGATA 0.014% NA yes 5 −5.101 CTGATC 0.012% NA yes 5 −2.539 CTGATG0.016%  0.235 yes 5 −2.001 CTGCAT 0.019% NA no 5 −1.930 CTGCCT 0.008% 0.310 no 5 −1.990 CTGCGT 0.011%  0.423 no 5 −0.420 CTGCTA 0.010% NA no5 −1.068 CTGCTC 0.008%  0.334 no 5 −0.467 CTGCTG 0.013%  0.333 no 5−1.002 CTGGAA 0.016% NA no 5 1.036 CTGGAC 0.009% NA no 5 −0.724 CTGGAG0.017% NA no 5 −0.675 CTGGCA 0.016% NA no 5 0.172 CTGGCC 0.007% NA no 50.854 CTGGCG 0.013%  0.317 no 5 −0.298 CTGGGA 0.015%  0.115 no 5 −0.526CTGGGC 0.010% NA no 5 −0.027 CTGGGG 0.015% NA no 5 0.165 CTGTAT 0.012%NA no 5 −0.148 CTGTCT 0.008% NA no 5 0.684 CTGTGT 0.013% −0.177 no 52.444 CTGTTA 0.011% NA no 5 1.526 CTGTTC 0.008% NA no 5 −0.152 CTGTTG0.013% NA no 5 0.424 CTTAAT 0.011% −0.598 no 5 −1.921 CTTACT 0.010% NAno 5 −3.914 CTTAGT 0.010% −0.774 no 5 −7.156 CTTATA 0.011% −0.791 no 5−1.113 CTTATC 0.009% NA no 5 −3.039 CTTATG 0.012% −0.307 no 5 −1.075CTTCAT 0.008% NA no 5 0.389 CTTCCT 0.005%  0.298 no 5 1.368 CTTCGT0.007%  0.413 no 5 1.632 CTTCTA 0.008% −0.363 no 5 −0.565 CTTCTC 0.006%NA no 5 −0.968 CTTCTG 0.006%  0.309 no 5 −0.153 CTTGAA 0.013% NA no 50.006 CTTGAC 0.008% NA no 5 2.668 CTTGAG 0.012% NA no 5 −0.635 CTTGCA0.011% −0.191 no 5 −0.758 CTTGCG 0.013% NA no 5 −1.131 CTTGGA 0.019% NAno 5 −0.476 CTTGGC 0.011% NA no 5 −0.152 CTTGGG 0.013% NA no 5 −0.037CTTTAT 0.008% −0.753 no 5 −1.800 CTTTCT 0.004% NA no 5 −3.554 CTTTGT0.010% −0.303 no 5 −0.930 CTTTTA 0.011% −1.061 no 5 −2.689 CTTTTG 0.007%−0.322 no 5 1.020 GAAAAA 0.073% NA no 5 −1.912 GAAAAC 0.063%  0.303 no 5−0.762 GAAAAG 0.070% NA no 5 −0.456 GAAACA 0.067% NA no 5 −1.225 GAAACC0.039%  0.340 no 5 −0.658 GAAACG 0.049%  0.468 no 5 −0.535 GAAAGA 0.067% 0.346 no 5 −1.562 GAAAGC 0.048%  0.298 no 5 −0.957 GAAAGG 0.074% −0.141no 5 −0.732 GAACAA 0.071%  0.467 no 5 −1.161 GAACAC 0.043%  0.417 no 5−0.564 GAACAG 0.054% NA no 5 −1.772 GAACCA 0.036%  0.363 no 5 −0.524GAACCC 0.022% NA no 5 −0.257 GAACCG 0.032%  0.585 no 5 0.157 GAACGA0.046%  0.642 no 5 −0.098 GAACGC 0.032%  0.703 no 5 −0.930 GAACGG 0.056% 0.441 no 5 −0.213 GAATAA 0.067% NA no 5 −2.770 GAATAC 0.037%  0.406 no5 −1.138 GAATAG 0.066% −0.335 no 5 −1.653 GAATCA 0.043% NA no 5 −0.566GAATCC 0.023%  0.470 no 5 −0.292 GAATCG 0.041%  0.586 no 5 0.067 GAATGA0.061% NA no 5 −2.111 GAATGC 0.039%  0.197 no 5 −0.256 GAATGG 0.060% NAno 5 −0.599 GACAAT 0.030% NA no 5 0.539 GACACT 0.021%  0.281 no 5 −0.605GACAGT 0.040% NA no 5 −1.244 GACATA 0.032% NA no 5 −0.663 GACATC 0.023% 0.682 no 5 0.415 GACATG 0.029%  0.262 no 5 0.258 GACCAT 0.024%  0.380no 5 −0.090 GACCCT 0.018%  0.545 no 5 −0.032 GACCGT 0.017%  0.536 no 50.344 GACCTA 0.020% NA no 5 1.043 GACCTC 0.014%  0.384 no 5 −0.229GACCTG 0.016%  0.664 no 5 0.902 GACGAA 0.034%  0.718 no 5 0.028 GACGAC0.027%  0.846 no 5 −0.223 GACGAG 0.038%  0.529 no 5 −0.271 GACGCA 0.032% 0.514 no 5 −1.035 GACGCC 0.011%  0.663 no 5 −0.620 GACGCG 0.024%  0.821no 5 0.142 GACGGA 0.041%  0.873 no 5 −0.316 GACGGC 0.021%  0.724 no 50.421 GACGGG 0.032%  0.470 no 5 0.153 GACTAT 0.022% NA no 5 −0.196GACTCT 0.014%  0.397 no 5 −1.331 GACTGT 0.021%  0.323 no 5 0.052 GACTTA0.027% NA no 5 −0.558 GACTTC 0.016%  0.445 no 5 −0.267 GACTTG 0.021% 0.168 no 5 0.013 GAGAAT 0.062%  0.309 no 5 −1.153 GAGACT 0.033%  0.490no 5 −0.030 GAGAGT 0.050%  0.247 no 5 −1.343 GAGATA 0.052% NA no 5−0.848 GAGATC 0.023%  0.477 no 5 −1.372 GAGATG 0.050%  0.327 no 5 −0.289GAGCAT 0.034% NA no 5 −0.396 GAGCCT 0.014% NA no 5 −0.557 GAGCGT 0.028% 0.305 no 5 −0.085 GAGCTA 0.031% −0.294 no 5 −0.698 GAGCTC 0.016% NA no5 −0.583 GAGCTG 0.024%  0.270 no 5 0.367 GAGGAA 0.070%  0.410 no 5−0.457 GAGGAC 0.032%  0.626 no 5 −0.912 GAGGAG 0.056%  0.247 no 5 −0.609GAGGCA 0.043% NA no 5 −1.224 GAGGCC 0.025%  0.380 no 5 −0.061 GAGGCG0.031%  0.332 no 5 −0.424 GAGGGA 0.058% NA no 5 −4.266 GAGGGC 0.029%−0.084 no 5 −2.555 GAGGGG 0.053% −0.144 no 5 −3.081 GAGTAT 0.039% NA no5 −1.700 GAGTCT 0.019%  0.271 no 5 −0.853 GAGTGT 0.030% NA no 5 −0.801GAGTTA 0.033% −0.179 no 5 −2.132 GAGTTC 0.023%  0.210 no 5 −0.912 GAGTTG0.028%  0.132 no 5 0.633 GATAAT 0.036% NA no 5 −2.443 GATACT 0.018% 0.225 no 5 −1.391 GATAGT 0.026% −0.235 no 5 −6.217 GATATA 0.037% NA no5 −2.538 GATATC 0.030% NA no 5 −2.461 GATATG 0.035% NA no 5 −0.826GATCAT 0.020%  0.298 no 5 −1.305 GATCCT 0.013%  0.275 no 5 −0.810 GATCGT0.019%  0.458 no 5 −0.584 GATCTA 0.021% NA no 5 −1.813 GATCTC 0.012% NAno 5 −1.894 GATCTG 0.025%  0.385 no 5 0.068 GATGAA 0.052%  0.510 no 5−0.891 GATGAC 0.018%  0.643 no 5 0.550 GATGAG 0.024% NA no 5 −0.869GATGCA 0.036%  0.205 no 5 −1.369 GATGCC 0.013%  0.546 no 5 0.690 GATGCG0.021%  0.540 no 5 −0.126 GATGGA 0.033%  0.664 no 5 0.483 GATGGC 0.018% 0.576 no 5 0.448 GATGGG 0.034%  0.131 no 5 −0.136 GATTAT 0.020% NA no 5−3.377 GATTCT 0.013%  0.273 no 5 −4.732 GATTGT 0.022% NA no 5 −2.355GATTTA 0.033% NA no 5 −3.989 GATTTC 0.021% NA no 5 −3.935 GATTTG 0.023%NA no 5 −0.041 GCAAAA 0.051% NA no 5 −1.794 GCAAAC 0.033%  0.251 no 5−1.201 GCAAAG 0.054% NA no 5 −0.704 GCAACA 0.042%  0.306 no 5 −0.302GCAACC 0.019%  0.106 no 5 −0.899 GCAACG 0.035%  0.392 no 5 0.324 GCAAGA0.047%  0.891 no 5 −0.150 GCAAGC 0.038%  0.195 no 5 −0.964 GCAAGG 0.039%NA no 5 −1.281 GCACAA 0.033% NA no 5 −1.175 GCACAC 0.027% NA no 5 −0.308GCACAG 0.028% NA no 5 −0.687 GCACCA 0.029% −0.116 no 5 −0.412 GCACCC0.012% −0.117 no 5 −1.725 GCACCG 0.020% NA no 5 0.718 GCACGA 0.033% NAno 5 −0.733 GCACGC 0.022% NA no 5 −0.224 GCACGG 0.028%  0.164 no 5−0.404 GCATAA 0.037% −0.153 no 5 −1.497 GCATAC 0.022% NA no 5 −1.032GCATAG 0.036% −0.161 no 5 −0.258 GCATCA 0.021% NA no 5 0.441 GCATCC0.012% NA no 5 0.670 GCATCG 0.022% NA no 5 −0.098 GCATGA 0.035%  0.253no 5 −0.535 GCATGC 0.018% NA no 5 −0.325 GCATGG 0.035%  0.097 no 5−0.014 GCCAAT 0.023% NA no 5 −0.619 GCCACT 0.017% NA no 5 −0.735 GCCAGT0.022% −0.227 no 5 1.500 GCCATA 0.019% −0.395 no 5 −1.324 GCCATC 0.015%NA no 5 −0.140 GCCATG 0.021% NA no 5 0.377 GCCCAT 0.017% NA no 5 −0.072GCCCGT 0.012% NA no 5 −0.015 GCCCTA 0.009% −0.425 no 5 −0.434 GCCCTC0.009% NA no 5 −0.362 GCCCTG 0.011% NA no 5 0.271 GCCGAA 0.027% NA no 5−0.995 GCCGAC 0.014%  0.435 no 5 −0.378 GCCGAG 0.022% NA no 5 0.343GCCGCA 0.018% NA no 5 −0.175 GCCGCC 0.016% NA no 5 −1.112 GCCGCG 0.017% 0.487 no 5 1.475 GCCGGA 0.023%  0.428 no 5 0.006 GCCGGC 0.013% NA no 5−0.237 GCCGGG 0.022%  0.409 no 5 0.540 GCCTAT 0.016% −0.310 no 5 −0.958GCCTCT 0.009% NA no 5 −0.415 GCCTGT 0.014% NA no 5 0.090 GCCTTA 0.016%−0.481 no 5 −1.227 GCCTTC 0.010% NA no 5 −0.560 GCCTTG 0.015% NA no 50.114 GCGAAT 0.037% NA no 5 0.140 GCGACT 0.023%  0.434 no 5 0.664 GCGAGT0.026% NA no 5 0.903 GCGATA 0.032% NA no 5 −0.079 GCGATC 0.015%  0.474no 5 −0.188 GCGATG 0.023%  0.320 no 5 0.666 GCGCAT 0.020% NA no 5 0.153GCGCCT 0.011%  0.298 no 5 −0.807 GCGCGT 0.016%  0.285 no 5 −1.638 GCGCTA0.019% NA no 5 −0.341 GCGCTC 0.014% NA no 5 0.385 GCGCTG 0.020%  0.251no 5 −0.476 GCGGAA 0.040%  0.461 no 5 −0.051 GCGGAC 0.021%  0.725 no 5−0.390 GCGGAG 0.036%  0.346 no 5 −0.355 GCGGCA 0.025% NA no 5 0.120GCGGCC 0.015% NA no 5 0.790 GCGGCG 0.027%  0.555 no 5 1.289 GCGGGA0.042%  0.461 no 5 −0.986 GCGGGC 0.020%  0.289 no 5 −1.162 GCGGGG 0.030% 0.178 no 5 −0.662 GCGTAT 0.019% NA no 5 −1.712 GCGTCT 0.011%  0.302 no5 −1.378 GCGTGT 0.017% NA no 5 −1.271 GCGTTA 0.016% NA no 5 −0.524GCGTTC 0.012%  0.447 no 5 −0.686 GCGTTG 0.014%  0.149 no 5 −0.045 GCTAAT0.019% −0.321 no 5 −4.088 GCTACT 0.013% NA no 5 −1.692 GCTAGT 0.017%−0.474 no 5 −7.760 GCTATA 0.024% −0.534 no 5 −1.898 GCTATC 0.011% NA no5 −2.675 GCTATG 0.015% −0.251 no 5 1.611 GCTCAT 0.017% NA no 5 −1.340GCTCCT 0.011% NA no 5 −0.085 GCTCGT 0.014% NA no 5 0.090 GCTCTA 0.020%−0.349 no 5 −3.023 GCTCTC 0.013% NA no 5 −0.873 GCTCTG 0.016% NA no 50.288 GCTGAA 0.034% NA no 5 0.186 GCTGAC 0.017%  0.488 no 5 0.663 GCTGAG0.024% NA no 5 −0.329 GCTGCA 0.021%  0.115 no 5 −0.911 GCTGCC 0.008% 0.179 no 5 2.076 GCTGCG 0.021%  0.446 no 5 −0.124 GCTGGA 0.028% NA no 5−0.633 GCTGGC 0.013% NA no 5 0.510 GCTGGG 0.025% −0.216 no 5 0.086GCTTAT 0.018% −0.369 no 5 −2.526 GCTTCT 0.008% NA no 5 −1.708 GCTTGT0.022% NA no 5 0.587 GCTTTA 0.017% −0.795 no 5 −2.826 GCTTTC 0.011% NAno 5 −1.505 GCTTTG 0.016% −0.241 no 5 −0.412 GGCAAA 0.047%  0.128 no 5−0.459 GGCAAC 0.026%  0.283 no 5 −0.188 GGCAAG 0.036%  0.398 no 5 0.412GGCACA 0.030% −0.086 no 5 −0.271 GGCACC 0.015% −0.171 no 5 0.260 GGCACG0.024% NA no 5 −0.495 GGCAGA 0.041%  0.210 no 5 0.887 GGCAGC 0.029% NAno 5 −0.243 GGCAGG 0.043% −0.229 no 5 0.010 GGCCAA 0.028% NA no 5 0.253GGCCAC 0.019% NA no 5 0.005 GGCCAG 0.025% NA no 5 −0.011 GGCCCA 0.015%NA no 5 −0.133 GGCCCC 0.012% NA no 5 −0.295 GGCCCG 0.014% NA no 5 0.293GGCCGA 0.026%  0.204 no 5 0.231 GGCCGC 0.009%  0.202 no 5 2.060 GGCCGG0.019%  0.129 no 5 −0.641 GGCTAA 0.027% −0.257 no 5 0.240 GGCTAC 0.019%NA no 5 −0.109 GGCTAG 0.022% −0.519 no 5 0.275 GGCTCA 0.016% −0.282 no 50.232 GGCTCC 0.009% NA no 5 3.465 GGCTCG 0.019% NA no 5 1.424 GGCTGA0.022%  0.192 no 5 0.203 GGCTGC 0.015%  0.151 no 5 0.186 GGCTGG 0.028%−0.221 no 5 0.177 GGGAAA 0.073% −0.218 no 5 −0.163 GGGAAC 0.046%  0.211no 5 0.186 GGGAAG 0.065% NA no 5 −0.359 GGGACA 0.050% NA no 5 0.256GGGACC 0.027%  0.292 no 5 0.047 GGGACG 0.039%  0.266 no 5 −0.327 GGGAGA0.053% NA no 5 0.171 GGGAGC 0.030%  0.194 no 5 0.400 GGGAGG 0.045%−0.461 no 5 −0.705 GGGCAA 0.044% −0.271 no 5 −0.283 GGGCAC 0.031% NA no5 0.330 GGGCAG 0.037% −0.367 no 5 −0.572 GGGCCA 0.028% NA no 5 0.059GGGCCC 0.016% NA no 5 0.440 GGGCCG 0.023% NA no 5 −0.113 GGGCGA 0.036%NA no 5 −0.193 GGGCGC 0.023%  0.189 no 5 −0.169 GGGCGG 0.028% −0.213 no5 0.023 GGGTAA 0.063% −0.710 no 5 −1.042 GGGTAC 0.031% −0.297 no 5−0.338 GGGTAG 0.042% −0.786 no 5 0.223 GGGTCA 0.031% −0.432 no 5 0.385GGGTCC 0.019% NA no 5 0.232 GGGTCG 0.024% NA no 5 −0.370 GGGTGA 0.031%−0.361 no 5 0.084 GGGTGC 0.027% −0.248 no 5 −0.622 GGGTGG 0.039% −0.643no 5 −0.238 GGTAAA 0.067% −0.588 no 5 0.380 GGTAAC 0.035% −0.330 no 50.469 GGTAAG 0.047% −0.770 no 5 −1.643 GGTACA 0.041% −0.359 no 5 0.125GGTACG 0.029% NA no 5 −0.411 GGTAGA 0.040% −0.530 no 5 −0.432 GGTAGC0.028% −0.532 no 5 −0.268 GGTAGG 0.039% −0.818 no 5 −3.067 GGTCAA 0.038%NA no 5 0.106 GGTCAC 0.026% NA no 5 0.375 GGTCAG 0.032% −0.351 no 5−0.019 GGTCCA 0.017% NA no 5 −0.107 GGTCCC 0.009% NA no 5 0.610 GGTCCG0.010% NA no 5 −0.116 GGTCGA 0.031% NA no 5 0.781 GGTCGC 0.017%  0.211no 5 −0.479 GGTCGG 0.021% NA no 5 −0.400 GGTTAA 0.042% −0.569 no 5 0.857GGTTAC 0.021% −0.225 no 5 0.462 GGTTAG 0.038% −0.781 no 5 −0.483 GGTTCA0.025% −0.261 no 5 0.137 GGTTCC 0.006% NA no 5 −1.212 GGTTCG 0.019% NAno 5 −1.113 GGTTGA 0.031% −0.204 no 5 0.084 GGTTGC 0.016% −0.236 no 50.246 GGTTGG 0.027% −0.324 no 5 −0.233 GTAAAA 0.060% −0.504 yes 5 −5.354GTAAAC 0.044% −0.319 yes 5 −4.406 GTAAAG 0.047% −0.374 yes 5 −3.346GTAACA 0.040% −0.466 yes 5 −4.312 GTAACC 0.027% NA yes 5 −3.350 GTAACG0.040% NA yes 5 −2.749 GTAAGA 0.047% −0.374 yes 5 −4.868 GTAAGC 0.033%−0.425 yes 5 −5.240 GTAAGG 0.046% −0.549 yes 5 −5.149 GTACAA 0.033%−0.338 no 5 −2.376 GTACAC 0.027% NA no 5 −1.926 GTACAG 0.028% −0.323 no5 −0.605 GTACCA 0.022% NA no 5 −0.815 GTACCC 0.011% NA no 5 −0.631GTACCG 0.018%  0.241 no 5 −0.081 GTACGA 0.023% NA no 5 −0.940 GTACGC0.017% NA no 5 0.275 GTACGG 0.026%  0.162 no 5 −0.333 GTATAA 0.040%−0.642 no 5 −4.297 GTATAC 0.025% NA no 5 −2.689 GTATAG 0.026% −0.715 no5 −1.271 GTATCA 0.029% −0.292 no 5 −1.926 GTATCC 0.017% NA no 5 0.022GTATCG 0.021% NA no 5 −0.770 GTATGA 0.037% NA no 5 −2.042 GTATGC 0.025%−0.144 no 5 −0.688 GTATGG 0.030% −0.214 no 5 −0.812 GTCAAT 0.025% NA no5 −1.344 GTCACT 0.018% NA no 5 0.785 GTCAGT 0.032% −0.308 no 5 −1.632GTCATA 0.028% NA no 5 −0.727 GTCATC 0.018%  0.352 no 5 −0.151 GTCATG0.025% NA no 5 −0.051 GTCCAT 0.018% NA no 5 −0.880 GTCCCT 0.008% NA no 5−0.675 GTCCTA 0.013% NA no 5 −1.202 GTCCTC 0.007% NA no 5 −5.098 GTCCTG0.010%  0.400 no 5 −2.620 GTCGAA 0.039% NA no 5 −1.055 GTCGAC 0.020% 0.686 no 5 0.900 GTCGAG 0.026% NA no 5 −0.778 GTCGCA 0.019% NA no 5−1.538 GTCGCC 0.010%  0.441 no 5 −0.453 GTCGCG 0.022%  0.497 no 5 −0.592GTCGGA 0.024%  0.394 no 5 −0.690 GTCGGC 0.020%  0.440 no 5 1.670 GTCGGG0.025%  0.312 no 5 0.431 GTCTAT 0.020% NA no 5 −0.762 GTCTCT 0.011% NAno 5 −0.765 GTCTGT 0.016% NA no 5 −1.155 GTCTTA 0.013% −0.386 no 5−1.347 GTCTTC 0.008%  0.325 no 5 −2.003 GTCTTG 0.019% NA no 5 −0.336GTGAAT 0.040%  0.199 yes 5 −2.115 GTGACT 0.020%  0.221 yes 5 −2.125GTGAGT 0.039% NA yes 5 −3.111 GTGATA 0.035% −0.165 yes 5 −2.428 GTGATC0.023%  0.249 yes 5 −3.472 GTGATG 0.033%  0.235 yes 5 −3.399 GTGCAT0.025% −0.441 no 5 −0.232 GTGCCT 0.011% −0.422 no 5 −0.446 GTGCGT 0.022%−0.172 no 5 −0.824 GTGCTA 0.020% −0.525 no 5 −0.885 GTGCTC 0.013% −0.092no 5 −0.179 GTGCTG 0.020% NA no 5 −1.182 GTGGAA 0.048%  0.587 no 5−0.533 GTGGAC 0.031%  0.622 no 5 −0.439 GTGGAG 0.031%  0.512 no 5 0.284GTGGCA 0.039% NA no 5 −0.129 GTGGCC 0.017% NA no 5 1.182 GTGGCG 0.024% 0.308 no 5 0.828 GTGGGA 0.043%  0.153 no 5 −1.383 GTGGGC 0.025% −0.140no 5 −0.349 GTGGGG 0.034% −0.214 no 5 −0.841 GTGTAT 0.019% −0.295 no 5−0.725 GTGTCT 0.019% NA no 5 −1.105 GTGTGT 0.023% −0.159 no 5 −0.949GTGTTA 0.024% −0.436 no 5 −0.211 GTGTTC 0.017% NA no 5 −0.341 GTGTTG0.021% −0.111 no 5 0.886 GTTAAT 0.026% −0.287 no 5 −3.781 GTTACT 0.017%NA no 5 −2.622 GTTAGT 0.027% −0.707 no 5 −8.956 GTTATA 0.021% −0.314 no5 −3.026 GTTATC 0.023%  0.149 no 5 −3.730 GTTATG 0.021% −0.147 no 5−1.779 GTTCAT 0.024%  0.162 no 5 −0.873 GTTCCT 0.005% NA no 5 0.484GTTCGT 0.016%  0.428 no 5 −0.689 GTTCTA 0.017% NA no 5 −2.578 GTTCTC0.011%  0.246 no 5 −2.189 GTTCTG 0.017%  0.165 no 5 0.789 GTTGAA 0.037% 0.175 no 5 −1.037 GTTGAC 0.014%  0.362 no 5 −1.330 GTTGAG 0.026% −0.218no 5 0.387 GTTGCA 0.025% NA no 5 −1.266 GTTGCC 0.014%  0.338 no 5 −0.182GTTGCG 0.018%  0.366 no 5 0.269 GTTGGA 0.032%  0.175 no 5 0.049 GTTGGC0.017%  0.180 no 5 −0.486 GTTGGG 0.024% −0.182 no 5 −0.890 GTTTAT 0.017%−0.244 no 5 −2.759 GTTTCT 0.015% NA no 5 −3.512 GTTTGT 0.022% NA no 5−2.699 GTTTTA 0.020% −0.312 no 5 −3.897 GTTTTC 0.012%  0.142 no 5 −6.195GTTTTG 0.020% −0.196 no 5 −0.776 TACAAA 0.034% NA no 5 −1.744 TACAAC0.019% NA no 5 −0.751 TACAAG 0.035% NA no 5 −0.198 TACACA 0.026% NA no 5−0.939 TACACC 0.014% NA no 5 −1.353 TACACG 0.023%  0.299 no 5 −0.284TACAGA 0.029% NA no 5 −0.020 TACAGC 0.020% NA no 5 0.419 TACAGG 0.024%−0.303 no 5 −0.484 TACCAA 0.020% NA no 5 −0.661 TACCAC 0.010% NA no 5−1.428 TACCAG 0.018% −0.081 no 5 −0.955 TACCCA 0.012% −0.192 no 5 −0.595TACCCC 0.010% −0.148 no 5 −1.060 TACCCG 0.006%  0.302 no 5 −1.404 TACCGA0.013%  0.439 no 5 −0.416 TACCGC 0.015% NA no 5 −0.105 TACCGG 0.014% 0.450 no 5 −0.806 TACTAA 0.014% NA no 5 −2.034 TACTAC 0.010% NA no 5−1.549 TACTAG 0.017% −0.521 no 5 −1.505 TACTCA 0.020% NA no 5 −2.617TACTCC 0.007% NA no 5 −0.371 TACTCG 0.013%  0.268 no 5 −0.441 TACTGA0.018% NA no 5 −1.449 TACTGC 0.015%  0.131 no 5 −0.786 TACTGG 0.015% NAno 5 −0.002 TAGAAA 0.039% −0.457 no 5 −6.589 TAGAAC 0.016% NA no 5−3.798 TAGAAG 0.041% −0.334 no 5 −2.207 TAGACA 0.022% −0.586 no 5 −5.210TAGACC 0.014% −0.252 no 5 −3.376 TAGACG 0.023% NA no 5 −2.794 TAGAGA0.026% −0.424 no 5 −4.534 TAGAGC 0.010% NA no 5 −3.536 TAGAGG 0.033%−0.452 no 5 −4.480 TAGCAA 0.025% −0.545 no 5 −6.255 TAGCAC 0.016% −0.451no 5 −7.027 TAGCAG 0.020% −0.644 no 5 −1.294 TAGCCA 0.015% −0.561 no 5−5.679 TAGCCC 0.009% −0.599 no 5 −4.306 TAGCCG 0.021% NA no 5 −0.532TAGCGA 0.019% NA no 5 −4.953 TAGCGC 0.008% NA no 5 −2.377 TAGCGG 0.025%−0.179 no 5 −0.275 TAGTAA 0.026% −0.812 no 5 −8.863 TAGTAC 0.017% −0.557no 5 −7.798 TAGTAG 0.025% −0.938 no 5 −4.603 TAGTCA 0.015% −0.684 no 5−4.130 TAGTCC 0.007% −0.447 no 5 −4.568 TAGTCG 0.015% NA no 5 −5.048TAGTGA 0.021% −0.578 no 5 −8.614 TAGTGC 0.014% −0.352 no 5 −4.905 TAGTGG0.021% −0.589 no 5 −4.232 TATAAA 0.035% −0.504 no 5 −4.694 TATAAC 0.025%−0.328 no 5 −4.439 TATAAG 0.037% −0.518 no 5 −1.982 TATACA 0.024% NA no5 −6.137 TATACC 0.010% −0.224 no 5 −3.607 TATACG 0.020% NA no 5 −1.105TATAGA 0.025% −0.447 no 5 −5.487 TATAGC 0.023% −0.401 no 5 −9.389 TATAGG0.025% −0.771 no 5 −3.740 TATCAA 0.019% NA no 5 −3.486 TATCAC 0.018% NAno 5 −3.211 TATCAG 0.020% −0.379 no 5 −2.726 TATCCA 0.016% NA no 5−2.892 TATCCC 0.008% −0.329 no 5 −1.310 TATCCG 0.009%  0.426 no 5 −0.178TATCGA 0.019% NA no 5 −0.977 TATCGC 0.017% NA no 5 −1.008 TATCGG 0.014% 0.215 no 5 −1.506 TATTAA 0.037% −0.602 no 5 −5.478 TATTAC 0.023% −0.356no 5 −3.997 TATTAG 0.024% −0.781 no 5 −3.825 TATTCA 0.025% NA no 5−4.573 TATTCC 0.005% −0.329 no 5 −5.515 TATTCG 0.011% NA no 5 −1.459TATTGA 0.028% NA no 5 −4.403 TATTGC 0.021% −0.358 no 5 −4.090 TATTGG0.025% −0.256 no 5 −1.227 TCCAAA 0.025% NA no 5 −0.289 TCCAAC 0.012% NAno 5 0.190 TCCAAG 0.021% NA no 5 −0.417 TCCACA 0.016% NA no 5 0.579TCCACC 0.011% −0.225 no 5 −0.574 TCCACG 0.013%  0.537 no 5 −0.677 TCCAGA0.025%  0.053 no 5 0.050 TCCAGC 0.013% NA no 5 0.101 TCCAGG 0.017% NA no5 −0.781 TCCCAA 0.013% −0.444 no 5 −0.474 TCCCAC 0.010% NA no 5 −2.680TCCCAG 0.014% −0.292 no 5 −1.114 TCCCCA 0.012% −0.476 no 5 0.763 TCCCCC0.005% −0.393 no 5 −0.635 TCCCCG 0.009%  0.350 no 5 0.046 TCCCGA 0.011%NA no 5 −0.342 TCCCGC 0.009% NA no 5 −0.775 TCCCGG 0.012%  0.401 no 51.328 TCCTAA 0.010% NA no 5 −1.571 TCCTAC 0.004% NA no 5 −1.401 TCCTAG0.005% −0.437 no 5 −0.513 TCCTCA 0.010% NA no 5 −0.458 TCCTCC 0.009% NAno 5 −0.145 TCCTCG 0.010%  0.623 no 5 0.593 TCCTGA 0.010% NA no 5 0.509TCCTGC 0.010%  0.484 no 5 0.942 TCCTGG 0.010%  0.335 no 5 −0.442 TCGAAA0.034% NA no 5 −0.872 TCGAAC 0.021%  0.477 no 5 −0.143 TCGAAG 0.035% 0.297 no 5 −0.951 TCGACA 0.018%  0.428 no 5 −1.033 TCGACC 0.013%  0.650no 5 0.297 TCGACG 0.015%  0.875 no 5 −1.137 TCGAGA 0.025%  0.467 no 51.436 TCGAGC 0.022%  0.449 no 5 −0.432 TCGAGG 0.027%  0.256 no 5 −0.282TCGCAA 0.026% NA no 5 0.831 TCGCAC 0.013%  0.502 no 5 −0.998 TCGCAG0.016% NA no 5 −0.069 TCGCCA 0.016%  0.422 no 5 −0.507 TCGCCC 0.005% 0.352 no 5 −0.672 TCGCCG 0.007%  0.911 no 5 0.036 TCGCGA 0.014%  0.661no 5 −0.336 TCGCGC 0.011%  0.674 no 5 −0.179 TCGCGG 0.022%  0.621 no 5−0.504 TCGTAA 0.027% NA no 5 −2.058 TCGTAC 0.013%  0.472 no 5 0.648TCGTAG 0.013% −0.318 no 5 −1.878 TCGTCA 0.012%  0.502 no 5 −0.100 TCGTCC0.008%  0.650 no 5 0.701 TCGTCG 0.012%  0.952 no 5 0.033 TCGTGA 0.018% 0.435 no 5 −0.519 TCGTGC 0.010%  0.216 no 5 −0.335 TCGTGG 0.017%  0.404no 5 0.453 TCTAAA 0.022% NA no 5 −3.197 TCTAAC 0.015% NA no 5 −3.877TCTAAG 0.017% −0.346 no 5 −1.726 TCTACA 0.015% NA no 5 −1.131 TCTACC0.006% NA no 5 −0.777 TCTACG 0.011%  0.646 no 5 0.472 TCTAGA 0.018% NAno 5 −4.489 TCTAGC 0.012% NA no 5 −4.016 TCTAGG 0.012% −0.561 no 5−4.521 TCTCAA 0.019% NA no 5 −2.451 TCTCAC 0.006% NA no 5 −0.333 TCTCAG0.021% NA no 5 −1.602 TCTCCA 0.013% −0.144 no 5 −0.625 TCTCCC 0.008% NAno 5 −1.035 TCTCCG 0.007%  0.647 no 5 0.334 TCTCGA 0.013%  0.385 no 5−0.680 TCTCGC 0.015%  0.475 no 5 −0.125 TCTCGG 0.012%  0.283 no 5 1.031TCTTAA 0.017% NA no 5 −4.390 TCTTAC 0.010% NA no 5 −2.830 TCTTAG 0.015%−0.622 no 5 −2.510 TCTTCA 0.013%  0.348 no 5 −0.233 TCTTCC 0.004% NA no5 −2.014 TCTTCG 0.008%  0.741 no 5 3.396 TCTTGA 0.018% NA no 5 −2.890TCTTGC 0.007% −0.251 no 5 −1.897 TCTTGG 0.017% NA no 5 0.655 TTCAAA0.031% NA no 5 −0.805 TTCAAC 0.019%  0.504 no 5 −0.794 TTCAAG 0.024% 0.257 no 5 0.367 TTCACA 0.017% NA no 5 −1.522 TTCACC 0.010%  0.229 no 50.986 TTCACG 0.014%  0.388 no 5 −0.429 TTCAGA 0.028% NA no 5 −0.116TTCAGC 0.013%  0.200 no 5 0.379 TTCAGG 0.022% −0.322 no 5 −0.183 TTCCAA0.016% NA no 5 −0.030 TTCCAG 0.013% −0.066 no 5 −0.407 TTCCCA 0.011%−0.468 no 5 −2.337 TTCCCG 0.007% NA no 5 −1.343 TTCCGA 0.011%  0.249 no5 −0.972 TTCCGC 0.007%  0.275 no 5 −0.268 TTCCGG 0.005%  0.489 no 51.161 TTCTAA 0.014% NA no 5 −2.612 TTCTAC 0.011%  0.436 no 5 −0.142TTCTAG 0.013% −0.396 no 5 −1.354 TTCTCA 0.011% NA no 5 −2.262 TTCTCC0.007%  0.170 no 5 0.765 TTCTCG 0.009%  0.383 no 5 −1.025 TTCTGA 0.015% 0.215 no 5 −0.870 TTCTGC 0.007%  0.286 no 5 −2.414 TTCTGG 0.013% NA no5 0.018 TTGAAA 0.033% NA yes 5 −4.030 TTGAAC 0.018%  0.310 yes 5 −3.608TTGAAG 0.025% NA yes 5 −1.958 TTGACA 0.025% NA yes 5 −2.711 TTGACC0.015%  0.275 yes 5 −0.405 TTGACG 0.015%  0.454 yes 5 −2.523 TTGAGA0.034% NA yes 5 −4.157 TTGAGC 0.018% NA yes 5 −4.963 TTGAGG 0.028%−0.328 yes 5 −3.720 TTGCAA 0.022% NA no 5 −2.424 TTGCAC 0.015% −0.183 no5 −1.474 TTGCAG 0.021% NA no 5 −0.307 TTGCCA 0.017% NA no 5 −0.548TTGCCC 0.009% NA no 5 0.299 TTGCCG 0.009%  0.568 no 5 1.067 TTGCGA0.022%  0.421 no 5 −0.172 TTGCGC 0.013%  0.383 no 5 −1.171 TTGCGG 0.017% 0.281 no 5 −0.356 TTGTAA 0.030% −0.266 no 5 −4.571 TTGTAC 0.018% NA no5 −3.284 TTGTAG 0.024% −0.529 no 5 −2.313 TTGTCA 0.019% NA no 5 −2.718TTGTCC 0.008% NA no 5 −1.316 TTGTCG 0.011%  0.393 no 5 −2.406 TTGTGA0.017% NA no 5 −1.559 TTGTGC 0.016% −0.151 no 5 −1.858 TTGTGG 0.018%−0.200 no 5 −1.023 TTTAAA 0.024% −0.374 no 5 −5.352 TTTAAC 0.020% −0.205no 5 −4.093 TTTAAG 0.027% −0.444 no 5 −1.160 TTTACA 0.019% NA no 5−3.337 TTTACC 0.011% NA no 5 −1.276 TTTACG 0.015% NA no 5 −1.019 TTTAGA0.022% −0.485 no 5 −6.601 TTTAGC 0.017% −0.551 no 5 −6.999 TTTAGG 0.024%−0.785 no 5 −5.226 TTTCAA 0.021% NA no 5 −2.008 TTTCAC 0.012% NA no 5−2.971 TTTCAG 0.018% −0.189 no 5 −4.757 TTTCCA 0.018% −0.218 no 5 −1.259TTTCCC 0.005% −0.179 no 5 −2.008 TTTCCG 0.009%  0.475 no 5 −0.553 TTTCGA0.014%  0.442 no 5 −1.799 TTTCGC 0.012%  0.453 no 5 −1.907 TTTCGG 0.019% 0.214 no 5 −2.131 TTTTAA 0.021% −0.387 no 5 −4.022 TTTTAC 0.015% −0.193no 5 −5.053 TTTTAG 0.025% −0.648 no 5 −6.442 TTTTCA 0.017% NA no 5−9.618 TTTTCC 0.005% −0.165 no 5 −3.637 TTTTCG 0.012%  0.251 no 5 −2.527TTTTGA 0.022% NA no 5 −5.532 TTTTGC 0.009% −0.331 no 5 −3.122 TTTTGG0.015% −0.268 no 5 −1.089 AACAAA 0.079% NA no 6 −1.223 AACAAC 0.045% 0.551 no 6 −0.435 AACAAG 0.066% NA no 6 −0.152 AACACA 0.041% NA no 6−0.450 AACACC 0.020% NA no 6 0.583 AACACG 0.039%  0.474 no 6 −0.449AACAGA 0.064%  0.537 no 6 −0.863 AACAGC 0.038% NA no 6 −0.176 AACAGG0.050% −0.274 no 6 −0.552 AACCAA 0.044%  0.403 no 6 −0.664 AACCAC 0.025%NA no 6 −0.872 AACCAG 0.026% NA no 6 −0.484 AACCCA 0.027% −0.352 no 6−0.786 AACCCC 0.017% −0.255 no 6 −0.008 AACCCG 0.020%  0.470 no 6 0.317AACCGA 0.027% NA no 6 −0.091 AACCGC 0.022% NA no 6 0.099 AACCGG 0.027% 0.439 no 6 −0.504 AACTAA 0.032% NA no 6 −2.020 AACTAC 0.022%  0.312 no6 −1.103 AACTAG 0.029% −0.317 no 6 −0.749 AACTCA 0.028% NA no 6 −1.181AACTCC 0.012% NA no 6 −1.754 AACTCG 0.027%  0.416 no 6 −0.043 AACTGA0.038% NA no 6 −0.866 AACTGC 0.024%  0.209 no 6 −1.788 AACTGG 0.033% NAno 6 −0.353 AAGAAA 0.100%  0.795 no 6 −1.070 AAGAAC 0.051%  0.630 no 6−0.752 AAGAAG 0.091%  0.591 no 6 −0.870 AAGACA 0.066%  0.424 no 6 −1.011AAGACC 0.032%  0.397 no 6 −0.096 AAGACG 0.043%  0.725 no 6 −0.365 AAGAGA0.071%  0.675 no 6 −2.059 AAGAGC 0.045%  0.394 no 6 −1.261 AAGAGG 0.074%NA no 6 −0.907 AAGCAA 0.051% NA no 6 −2.326 AAGCAC 0.040% NA no 6 −1.268AAGCAG 0.045% NA no 6 −0.556 AAGCCA 0.031% NA no 6 −1.117 AAGCCC 0.015%NA no 6 −0.267 AAGCCG 0.022%  0.355 no 6 0.761 AAGCGA 0.039%  0.418 no 60.113 AAGCGC 0.028%  0.435 no 6 −0.954 AAGCGG 0.043%  0.286 no 6 −0.174AAGTAA 0.070% NA no 6 −3.365 AAGTAC 0.030% NA no 6 −2.618 AAGTAG 0.058%−0.478 no 6 −2.525 AAGTCA 0.033% NA no 6 −2.071 AAGTCC 0.009% NA no 6−0.638 AAGTCG 0.026%  0.427 no 6 0.228 AAGTGA 0.053% NA no 6 −2.274AAGTGC 0.029% NA no 6 −1.434 AAGTGG 0.049% −0.168 no 6 −0.181 AATAAA0.066% −0.344 no 6 −3.830 AATAAC 0.026% NA no 6 −3.783 AATAAG 0.056%−0.292 no 6 −1.313 AATACA 0.046% NA no 6 −4.253 AATACC 0.012% NA no 6−2.592 AATACG 0.034% NA no 6 −0.468 AATAGA 0.048% NA no 6 −6.561 AATAGC0.025% NA no 6 −4.772 AATAGG 0.047% −0.629 no 6 −6.146 AATCAA 0.042% NAno 6 −2.974 AATCAC 0.033% NA no 6 −3.043 AATCAG 0.044% NA no 6 −2.719AATCCA 0.027% NA no 6 −1.675 AATCCC 0.008% −0.213 no 6 −3.348 AATCCG0.018%  0.457 no 6 0.042 AATCGA 0.030%  0.468 no 6 −2.530 AATCGC 0.021% 0.396 no 6 0.006 AATCGG 0.034%  0.266 no 6 −0.083 AATTAA 0.031% NA no 6−4.301 AATTAC 0.010% NA no 6 −3.265 AATTAG 0.026% −0.609 no 6 −3.921AATTCA 0.012% NA no 6 −6.142 AATTCC 0.002% −0.220 no 6 −4.851 AATTCG0.010%  0.321 no 6 −1.960 AATTGA 0.037% NA no 6 −3.507 AATTGC 0.012%−0.205 no 6 −1.931 AATTGG 0.026% NA no 6 −0.842 ACCAAA 0.041% NA no 6−1.640 ACCAAC 0.026% NA no 6 0.173 ACCAAG 0.039% NA no 6 −0.064 ACCACA0.025% NA no 6 −1.649 ACCACC 0.015% −0.424 no 6 −0.772 ACCACG 0.030% 0.371 no 6 −0.266 ACCAGA 0.032% NA no 6 0.760 ACCAGC 0.018% NA no 60.644 ACCAGG 0.038% NA no 6 0.447 ACCCAA 0.031% −0.146 no 6 −1.064ACCCAC 0.015% −0.138 no 6 −1.499 ACCCAG 0.023% −0.227 no 6 −0.827 ACCCCA0.016% −0.328 no 6 −1.261 ACCCCC 0.011% −0.181 no 6 −1.060 ACCCCG 0.016% 0.122 no 6 0.043 ACCCGA 0.022%  0.318 no 6 0.129 ACCCGC 0.015%  0.273no 6 −0.661 ACCCGG 0.022%  0.317 no 6 −0.080 ACCTAA 0.021% −0.587 no 6−1.676 ACCTAC 0.016% NA no 6 0.459 ACCTAG 0.020% −0.327 no 6 −0.439ACCTCA 0.018% NA no 6 −0.718 ACCTCC 0.011% NA no 6 0.266 ACCTCG 0.017% 0.548 no 6 −0.647 ACCTGA 0.027% NA no 6 −0.620 ACCTGC 0.016%  0.442 no6 0.784 ACCTGG 0.022%  0.352 no 6 −0.530 ACGAAA 0.059% NA no 6 −0.509ACGAAC 0.034%  0.473 no 6 −0.601 ACGAAG 0.054%  0.405 no 6 0.044 ACGACA0.033% NA no 6 −0.435 ACGACC 0.019%  0.415 no 6 −0.709 ACGACG 0.035% 0.724 no 6 −0.168 ACGAGA 0.054% NA no 6 0.255 ACGAGC 0.032%  0.325 no 6−1.146 ACGAGG 0.046%  0.215 no 6 −0.521 ACGCAA 0.033% NA no 6 −0.561ACGCAC 0.021% NA no 6 −1.187 ACGCAG 0.028% NA no 6 0.578 ACGCCA 0.030% 0.372 no 6 −0.027 ACGCCC 0.014%  0.323 no 6 −0.528 ACGCCG 0.019%  0.809no 6 0.736 ACGCGA 0.023%  0.485 no 6 0.189 ACGCGC 0.026%  0.608 no 6−0.105 ACGCGG 0.029%  0.600 no 6 0.058 ACGTAA 0.033% NA no 6 −2.273ACGTAC 0.021%  0.286 no 6 −1.357 ACGTAG 0.032% −0.390 no 6 −0.423 ACGTCA0.026% NA no 6 −0.306 ACGTCC 0.016%  0.553 no 6 −0.992 ACGTCG 0.019% 0.810 no 6 1.044 ACGTGA 0.031% NA no 6 0.058 ACGTGC 0.019%  0.195 no 60.168 ACGTGG 0.028%  0.352 no 6 −0.177 ACTAAA 0.040% −0.583 no 6 −2.421ACTAAC 0.028% NA no 6 −4.117 ACTAAG 0.040% −0.359 no 6 −0.554 ACTACA0.026% NA no 6 −1.668 ACTACC 0.016% −0.209 no 6 −1.170 ACTACG 0.026% 0.510 no 6 −0.436 ACTAGA 0.031% NA no 6 −4.202 ACTAGC 0.016% NA no 6−5.326 ACTAGG 0.027% −0.542 no 6 −3.660 ACTCAA 0.033% NA no 6 −5.224ACTCAC 0.020% NA no 6 −4.276 ACTCAG 0.030% NA no 6 −3.063 ACTCCA 0.021%−0.139 no 6 −1.530 ACTCCC 0.013% NA no 6 −2.385 ACTCCG 0.017%  0.602 no6 −0.524 ACTCGA 0.030% NA no 6 −2.188 ACTCGC 0.017%  0.389 no 6 −2.331ACTCGG 0.025%  0.290 no 6 −0.663 ACTTAA 0.032% −0.672 no 6 −2.935 ACTTAC0.018% NA no 6 −2.808 ACTTAG 0.028% −0.656 no 6 −2.578 ACTTCA 0.023% NAno 6 −2.397 ACTTCC 0.005% NA no 6 −1.028 ACTTCG 0.026%  0.621 no 6 0.417ACTTGA 0.024% NA no 6 −1.997 ACTTGC 0.010% −0.139 no 6 −1.414 ACTTGG0.024% NA no 6 −0.685 ATCAAA 0.056% NA no 6 −0.835 ATCAAC 0.029% NA no 6−0.314 ATCAAG 0.045% NA no 6 0.147 ATCACA 0.037% NA no 6 −0.680 ATCACC0.019% −0.206 no 6 −0.633 ATCACG 0.029%  0.259 no 6 0.279 ATCAGA 0.046%NA no 6 −0.826 ATCAGC 0.030% NA no 6 −2.575 ATCAGG 0.037% −0.262 no 6−0.642 ATCCAA 0.034% NA no 6 −0.925 ATCCAC 0.021% NA no 6 −0.263 ATCCAG0.028%  0.145 no 6 0.100 ATCCCA 0.022% −0.279 no 6 −0.105 ATCCCC 0.014%−0.303 no 6 −1.336 ATCCCG 0.017%  0.506 no 6 0.680 ATCCGA 0.027% NA no 60.176 ATCCGC 0.014% NA no 6 0.323 ATCCGG 0.020%  0.511 no 6 −1.276ATCTAA 0.034% NA no 6 −1.364 ATCTAC 0.021% NA no 6 −0.528 ATCTAG 0.021%−0.547 no 6 −0.354 ATCTCA 0.023% NA no 6 −1.512 ATCTCC 0.010% NA no 60.658 ATCTCG 0.022%  0.322 no 6 0.927 ATCTGA 0.027% NA no 6 −0.341ATCTGC 0.016%  0.286 no 6 −1.701 ATCTGG 0.031% NA no 6 −0.188 ATGAAA0.066% NA yes 6 −3.745 ATGAAC 0.046%  0.449 yes 6 −3.231 ATGAAG 0.064% 0.338 yes 6 −2.507 ATGACA 0.041% NA yes 6 −5.400 ATGACC 0.022%  0.325yes 6 −3.099 ATGACG 0.026%  0.544 yes 6 −2.841 ATGAGA 0.058% NA yes 6−4.763 ATGAGC 0.032% NA yes 6 −4.554 ATGAGG 0.061% −0.233 yes 6 −3.655ATGCAA 0.043% NA no 6 −3.871 ATGCAC 0.028% −0.109 no 6 −4.321 ATGCAG0.032% NA no 6 −0.954 ATGCCA 0.029%  0.121 no 6 −2.194 ATGCCC 0.017% NAno 6 −1.692 ATGCCG 0.017%  0.422 no 6 −0.635 ATGCGA 0.040% NA no 6−1.188 ATGCGC 0.024%  0.408 no 6 −1.314 ATGCGG 0.032%  0.291 no 6 −0.769ATGTAA 0.050% NA no 6 −3.819 ATGTAC 0.028% NA no 6 −2.984 ATGTAG 0.044%−0.544 no 6 −2.805 ATGTCA 0.032% NA no 6 −2.740 ATGTCC 0.014% NA no 6−1.365 ATGTCG 0.024%  0.397 no 6 −0.366 ATGTGA 0.040% NA no 6 −2.236ATGTGC 0.026% NA no 6 −2.607 ATGTGG 0.040% NA no 6 −0.587 ATTAAA 0.059%−0.520 no 6 −3.838 ATTAAC 0.034% NA no 6 −3.640 ATTAAG 0.047% −0.359 no6 −1.145 ATTACA 0.046% NA no 6 −3.134 ATTACC 0.019% −0.226 no 6 −0.545ATTACG 0.020% NA no 6 −0.823 ATTAGA 0.045% NA no 6 −6.264 ATTAGC 0.025%−0.441 no 6 −4.786 ATTAGG 0.036% −0.727 no 6 −6.758 ATTCAA 0.035% NA no6 −3.119 ATTCAC 0.021% NA no 6 −2.825 ATTCAG 0.031% NA no 6 −4.356ATTCCA 0.016% −0.152 no 6 −2.110 ATTCCG 0.009%  0.453 no 6 0.015 ATTCGA0.026% NA no 6 −1.285 ATTCGC 0.017%  0.453 no 6 −0.274 ATTCGG 0.024% 0.274 no 6 −0.292 ATTTAA 0.035% −0.490 no 6 −6.043 ATTTAC 0.021% NA no6 −4.089 ATTTAG 0.034% −0.668 no 6 −2.827 ATTTCA 0.030% NA no 6 −5.418ATTTCC 0.009% −0.330 no 6 −4.799 ATTTCG 0.024%  0.301 no 6 −1.362 ATTTGA0.033% NA no 6 −3.536 ATTTGC 0.023% −0.177 no 6 −3.379 ATTTGG 0.031% NAno 6 −1.002 CACAAA 0.030% −0.211 no 6 −0.771 CACAAC 0.019% NA no 6 0.539CACAAG 0.026% NA no 6 −0.359 CACACA 0.024% NA no 6 −2.081 CACACC 0.016%NA no 6 0.247 CACACG 0.020% NA no 6 0.003 CACAGA 0.022% NA no 6 −0.253CACAGC 0.019% −0.222 no 6 −0.260 CACAGG 0.026% −0.235 no 6 −0.779 CACCAA0.020% −0.265 no 6 −0.763 CACCAC 0.013% NA no 6 −0.990 CACCAG 0.017%−0.233 no 6 0.104 CACCCA 0.013% −0.268 no 6 −1.539 CACCCC 0.012% −0.179no 6 −1.296 CACCCG 0.012%  0.193 no 6 0.915 CACCGA 0.022% NA no 6 −0.286CACCGC 0.013% NA no 6 0.030 CACCGG 0.019%  0.390 no 6 −0.746 CACTAA0.024% −0.481 no 6 −2.068 CACTAC 0.011% NA no 6 −0.250 CACTAG 0.016%−0.509 no 6 −0.299 CACTCA 0.019% −0.208 no 6 −0.887 CACTCC 0.008% NA no6 −1.706 CACTCG 0.014% NA no 6 −0.577 CACTGA 0.013% NA no 6 −1.397CACTGC 0.010% NA no 6 0.823 CACTGG 0.019% NA no 6 0.426 CAGAAA 0.044% NAno 6 −1.080 CAGAAC 0.030%  0.200 no 6 −0.460 CAGAAG 0.044%  0.390 no 60.587 CAGACA 0.033% NA no 6 −1.182 CAGACC 0.014% NA no 6 −0.740 CAGACG0.026%  0.466 no 6 −0.530 CAGAGA 0.038%  0.349 no 6 −0.391 CAGAGC 0.022%NA no 6 −0.552 CAGAGG 0.039% NA no 6 0.289 CAGCAA 0.026% NA no 6 −0.836CAGCAC 0.016% NA no 6 −0.794 CAGCAG 0.022% NA no 6 −0.735 CAGCCA 0.018%−0.445 no 6 −1.254 CAGCCC 0.011% −0.242 no 6 3.943 CAGCCG 0.014% NA no 6−0.381 CAGCGA 0.021% NA no 6 −0.777 CAGCGC 0.017% NA no 6 0.405 CAGCGG0.025%  0.262 no 6 0.134 CAGTAA 0.036% −0.456 no 6 −1.590 CAGTAC 0.019%NA no 6 1.194 CAGTAG 0.027% −0.530 no 6 −0.331 CAGTCA 0.020% −0.297 no 6−0.655 CAGTCC 0.013% NA no 6 −0.147 CAGTCG 0.020%  0.213 no 6 −0.761CAGTGA 0.025% NA no 6 −0.735 CAGTGC 0.012% −0.163 no 6 −0.562 CAGTGG0.029% NA no 6 −0.249 CATAAA 0.029% −0.324 no 6 −2.097 CATAAC 0.021%−0.238 no 6 −2.125 CATAAG 0.035% NA no 6 −0.479 CATACA 0.021% NA no 6−1.533 CATACC 0.010% NA no 6 −1.021 CATACG 0.020% NA no 6 1.296 CATAGA0.024% NA no 6 −2.030 CATAGC 0.015% NA no 6 −3.406 CATAGG 0.023% −0.456no 6 −2.964 CATCAA 0.021% NA no 6 0.271 CATCAC 0.018% NA no 6 −0.493CATCAG 0.016% NA no 6 −0.703 CATCCA 0.012%  0.125 no 6 −0.239 CATCCC0.008% NA no 6 −0.847 CATCCG 0.010%  0.184 no 6 0.198 CATCGA 0.023% NAno 6 −0.618 CATCGC 0.016%  0.232 no 6 0.067 CATCGG 0.020%  0.420 no 6−0.054 CATTAA 0.018% −0.355 no 6 −2.843 CATTAC 0.015% NA no 6 −2.805CATTAG 0.017% −0.514 no 6 −3.177 CATTCA 0.015% NA no 6 −2.604 CATTCC0.006% NA no 6 −1.749 CATTCG 0.011%  0.186 no 6 1.072 CATTGA 0.016% NAno 6 −0.844 CATTGC 0.012% NA no 6 1.900 CATTGG 0.020% NA no 6 −1.491CCCAAA 0.018% −0.434 no 6 −2.557 CCCAAC 0.012% NA no 6 −0.519 CCCAAG0.017% NA no 6 −0.776 CCCACA 0.012% −0.150 no 6 −3.281 CCCACC 0.005%−0.429 no 6 0.806 CCCACG 0.008%  0.302 no 6 −0.005 CCCAGA 0.010% −0.243no 6 0.265 CCCAGC 0.012% −0.541 no 6 0.198 CCCAGG 0.010% −0.091 no 6−0.919 CCCCAA 0.010% −0.359 no 6 −3.543 CCCCAC 0.005% −0.155 no 6 −4.110CCCCAG 0.011% −0.423 no 6 −0.160 CCCCCA 0.010% −0.396 no 6 −1.610 CCCCCC0.004% −0.137 no 6 −3.894 CCCCCG 0.004%  0.128 no 6 0.494 CCCCGA 0.010%NA no 6 −1.287 CCCCGC 0.008%  0.197 no 6 −0.294 CCCCGG 0.007%  0.192 no6 −1.772 CCCTAA 0.012% −0.467 no 6 −2.684 CCCTAC 0.003% NA no 6 −2.166CCCTAG 0.005% −0.531 no 6 −1.334 CCCTCA 0.010% NA no 6 −1.825 CCCTCC0.005%  0.115 no 6 −1.343 CCCTCG 0.008%  0.365 no 6 −0.699 CCCTGA 0.012%NA no 6 0.587 CCCTGC 0.008%  0.317 no 6 0.904 CCCTGG 0.012%  0.134 no 60.020 CCGAAA 0.022% NA no 6 0.254 CCGAAC 0.016%  0.309 no 6 −0.653CCGAAG 0.017%  0.455 no 6 −1.615 CCGACA 0.016% NA no 6 −0.232 CCGACC0.008%  0.193 no 6 0.208 CCGACG 0.010%  0.786 no 6 −0.263 CCGAGA 0.020% 0.263 no 6 0.081 CCGAGC 0.012%  0.216 no 6 −0.027 CCGAGG 0.019%  0.358no 6 0.033 CCGCAA 0.003% NA no 6 −2.683 CCGCAC 0.014% NA no 6 −1.423CCGCAG 0.013% −0.179 no 6 0.287 CCGCCA 0.011% −0.119 no 6 −1.825 CCGCCC0.006% NA no 6 −1.404 CCGCCG 0.007%  0.387 no 6 0.270 CCGCGA 0.014% 0.583 no 6 −0.361 CCGCGC 0.008%  0.485 no 6 −1.506 CCGCGG 0.008%  0.662no 6 −0.293 CCGTAA 0.012% NA no 6 −0.303 CCGTAC 0.009% NA no 6 1.249CCGTAG 0.011% −0.348 no 6 −0.076 CCGTCA 0.010%  0.347 no 6 −0.858 CCGTCC0.009%  0.395 no 6 0.551 CCGTCG 0.008%  0.857 no 6 −0.255 CCGTGA 0.015% 0.356 no 6 −0.091 CCGTGC 0.008%  0.205 no 6 0.378 CCGTGG 0.014%  0.447no 6 0.216 CCTAAA 0.013% −0.562 no 6 −2.307 CCTAAC 0.006% −0.367 no 6−1.831 CCTAAG 0.011% −0.380 no 6 1.499 CCTACA 0.011% NA no 6 0.212CCTACC 0.006% NA no 6 −0.373 CCTACG 0.012%  0.382 no 6 0.262 CCTAGA0.010% −0.469 no 6 −5.503 CCTAGC 0.007% −0.608 no 6 −2.402 CCTAGG 0.010%−0.465 no 6 −3.453 CCTCAA 0.010% NA no 6 −1.196 CCTCAC 0.008% NA no 6−1.720 CCTCAG 0.012% NA no 6 −0.872 CCTCCA 0.011% NA no 6 −1.175 CCTCCC0.005% NA no 6 −1.838 CCTCCG 0.007%  0.532 no 6 0.464 CCTCGA 0.009% 0.378 no 6 −0.270 CCTCGC 0.010%  0.374 no 6 −1.018 CCTCGG 0.011%  0.483no 6 0.379 CCTTAA 0.013% −0.629 no 6 −3.250 CCTTAC 0.005% −0.322 no 6−2.738 CCTTAG 0.008% −0.773 no 6 −2.026 CCTTCA 0.008% NA no 6 −1.677CCTTCC 0.006% NA no 6 −0.883 CCTTCG 0.006%  0.414 no 6 0.015 CCTTGA0.008% NA no 6 −0.905 CCTTGC 0.005% NA no 6 0.222 CCTTGG 0.007%  0.141no 6 −0.611 CTCAAA 0.023% −0.488 no 6 0.380 CTCAAC 0.008% NA no 6 −1.472CTCAAG 0.014% NA no 6 0.634 CTCACA 0.014% NA no 6 −0.348 CTCACC 0.008%NA no 6 0.519 CTCACG 0.009% NA no 6 −0.693 CTCAGA 0.022% NA no 6 −1.547CTCAGC 0.008% NA no 6 −0.792 CTCAGG 0.016% −0.316 no 6 −0.412 CTCCAA0.012% NA no 6 0.477 CTCCAC 0.006% NA no 6 −0.726 CTCCAG 0.011% −0.112no 6 −0.419 CTCCCA 0.007% −0.225 no 6 −3.150 CTCCCC 0.006% −0.260 no 6−3.218 CTCCGA 0.008%  0.507 no 6 −0.550 CTCCGC 0.007%  0.458 no 6 −2.501CTCCGG 0.009%  0.532 no 6 −1.221 CTCTAA 0.012% −0.382 no 6 −2.334 CTCTAC0.009% NA no 6 −0.627 CTCTAG 0.009% −0.387 no 6 −1.260 CTCTCA 0.006% NAno 6 −0.599 CTCTCG 0.009%  0.264 no 6 −1.408 CTCTGA 0.014% NA no 6 0.324CTCTGC 0.013%  0.263 no 6 −1.298 CTCTGG 0.012% NA no 6 −0.087 CTGAAA0.022% NA yes 6 −2.700 CTGAAC 0.011% NA yes 6 −4.087 CTGAAG 0.023% 0.266 yes 6 −1.983 CTGACA 0.013% NA yes 6 −2.374 CTGACC 0.009%  0.264yes 6 −1.931 CTGACG 0.014%  0.522 yes 6 −2.443 CTGAGA 0.017% NA yes 6−2.198 CTGAGG 0.014% NA yes 6 −3.700 CTGCAA 0.020% NA no 6 −0.143 CTGCAC0.015%  0.260 no 6 0.900 CTGCAG 0.012% NA no 6 −0.984 CTGCCA 0.006% NAno 6 2.754 CTGCCC 0.010% NA no 6 −0.749 CTGCCG 0.011%  0.619 no 6 −0.021CTGCGA 0.019%  0.659 no 6 0.152 CTGCGC 0.010%  0.585 no 6 1.570 CTGCGG0.019%  0.581 no 6 0.797 CTGTAA 0.023% NA no 6 −0.148 CTGTAC 0.007% NAno 6 1.658 CTGTAG 0.013% −0.556 no 6 1.942 CTGTCA 0.010% NA no 6 −0.657CTGTCC 0.008%  0.214 no 6 1.759 CTGTCG 0.008%  0.540 no 6 1.654 CTGTGA0.014%  0.272 no 6 −0.346 CTGTGC 0.008% −0.312 no 6 −0.669 CTGTGG 0.014% 0.169 no 6 −0.424 CTTAAA 0.017% −0.879 no 6 −1.900 CTTAAC 0.012% −0.432no 6 −1.462 CTTAAG 0.019% −0.427 no 6 −0.539 CTTACA 0.012% −0.564 no 6−2.129 CTTACC 0.010% NA no 6 −1.288 CTTACG 0.009% NA no 6 −0.300 CTTAGA0.014% −0.503 no 6 −3.987 CTTAGG 0.017% −0.727 no 6 −4.087 CTTCAA 0.014%NA no 6 −0.449 CTTCAC 0.007% NA no 6 −1.351 CTTCAG 0.009% NA no 6 −1.926CTTCCA 0.008% NA no 6 1.026 CTTCCC 0.009% −0.231 no 6 −1.730 CTTCGA0.009%  0.509 no 6 −0.601 CTTCGC 0.009%  0.571 no 6 −0.222 CTTCGG 0.006% 0.540 no 6 −0.297 CTTTAA 0.014% −1.050 no 6 −4.048 CTTTAC 0.006% −0.372no 6 −2.111 CTTTAG 0.011% −0.855 no 6 −4.136 CTTTCA 0.009% −0.561 no 6−3.027 CTTTCC 0.005% −0.238 no 6 −2.440 CTTTCG 0.007% NA no 6 −0.773CTTTGA 0.010% NA no 6 −1.354 CTTTGC 0.005% −0.256 no 6 −0.927 CTTTGG0.011% NA no 6 0.375 GACAAA 0.048% NA no 6 −1.019 GACAAC 0.036%  0.513no 6 0.299 GACAAG 0.047%  0.288 no 6 −0.317 GACACA 0.040% NA no 6 −0.164GACACC 0.025% NA no 6 −0.184 GACACG 0.033%  0.493 no 6 −0.023 GACAGA0.048%  0.414 no 6 −0.131 GACAGC 0.036% NA no 6 0.088 GACAGG 0.042%−0.224 no 6 −0.521 GACCAA 0.033%  0.412 no 6 −0.634 GACCAC 0.020% NA no6 −0.639 GACCAG 0.027%  0.338 no 6 −0.990 GACCCA 0.021% NA no 6 −0.026GACCCC 0.014% NA no 6 0.042 GACCCG 0.015%  0.625 no 6 −0.042 GACCGA0.022%  0.598 no 6 −0.695 GACCGC 0.017%  0.342 no 6 1.073 GACCGG 0.026% 0.647 no 6 0.166 GACTAA 0.030% NA no 6 −0.387 GACTAC 0.018%  0.414 no 6−0.665 GACTAG 0.025% −0.304 no 6 0.221 GACTCA 0.027% NA no 6 −1.031GACTCC 0.012%  0.198 no 6 1.074 GACTCG 0.021%  0.502 no 6 0.492 GACTGA0.025%  0.472 no 6 −0.563 GACTGC 0.018%  0.515 no 6 0.507 GACTGG 0.025% 0.199 no 6 −0.051 GAGAAA 0.075%  0.302 no 6 −0.608 GAGAAC 0.046%  0.504no 6 −0.072 GAGAAG 0.064%  0.245 no 6 −0.118 GAGACA 0.042% NA no 6−0.990 GAGACC 0.025%  0.480 no 6 −0.090 GAGACG 0.036%  0.528 no 6 0.029GAGAGA 0.055%  0.355 no 6 −0.401 GAGAGC 0.035%  0.462 no 6 0.030 GAGAGG0.056% NA no 6 −0.680 GAGCAA 0.050% NA no 6 −0.602 GAGCAC 0.021% NA no 6−0.633 GAGCAG 0.030% NA no 6 −0.687 GAGCCA 0.028%  0.299 no 6 −0.128GAGCCC 0.012% NA no 6 −0.182 GAGCCG 0.021%  0.367 no 6 0.563 GAGCGA0.033%  0.483 no 6 −0.104 GAGCGC 0.023%  0.535 no 6 0.993 GAGCGG 0.025% 0.252 no 6 0.596 GAGTAA 0.059% NA no 6 −1.639 GAGTAC 0.030%  0.276 no 6−0.956 GAGTAG 0.040% −0.344 no 6 −0.575 GAGTCA 0.036% NA no 6 −1.241GAGTCC 0.016%  0.454 no 6 2.359 GAGTCG 0.023%  0.400 no 6 −1.485 GAGTGA0.049% NA no 6 −0.933 GAGTGC 0.023% NA no 6 −0.697 GAGTGG 0.046% NA no 60.097 GATAAA 0.046% NA no 6 −2.806 GATAAC 0.025% NA no 6 −2.792 GATAAG0.039% NA no 6 −0.480 GATACA 0.037% NA no 6 −1.321 GATACC 0.015%  0.232no 6 −0.654 GATACG 0.028%  0.389 no 6 0.151 GATAGA 0.036% NA no 6 −4.398GATAGC 0.031% NA no 6 −4.817 GATAGG 0.033% −0.688 no 6 −4.666 GATCAA0.035% NA no 6 −1.017 GATCAC 0.018% NA no 6 −1.087 GATCAG 0.030% −0.223no 6 −0.915 GATCCA 0.021%  0.400 no 6 −0.191 GATCCC 0.010% NA no 6−0.396 GATCCG 0.013%  0.488 no 6 −0.810 GATCGA 0.025%  0.518 no 6 0.807GATCGC 0.018%  0.392 no 6 0.474 GATCGG 0.024%  0.443 no 6 −0.459 GATTAA0.032% −0.297 no 6 −2.387 GATTAC 0.016% NA no 6 −2.926 GATTAG 0.028%−0.496 no 6 −2.360 GATTCA 0.017% NA no 6 −3.109 GATTCC 0.010%  0.223 no6 −2.216 GATTCG 0.015%  0.518 no 6 −1.842 GATTGA 0.035%  0.284 no 6−1.102 GATTGC 0.017%  0.123 no 6 0.027 GATTGG 0.031% NA no 6 0.014GCCAAA 0.039% −0.438 no 6 −0.555 GCCAAC 0.018% NA no 6 −1.562 GCCAAG0.018% NA no 6 0.564 GCCACA 0.023% NA no 6 −1.006 GCCACC 0.012% −0.311no 6 0.422 GCCACG 0.023% NA no 6 −0.096 GCCAGA 0.032%  0.072 no 6 −0.378GCCAGC 0.021% −0.294 no 6 −0.658 GCCAGG 0.026% −0.320 no 6 −0.140 GCCCAA0.020% −0.363 no 6 −0.822 GCCCAG 0.016% NA no 6 −0.433 GCCCCA 0.011%−0.238 no 6 −1.599 GCCCCC 0.007% −0.212 no 6 −1.362 GCCCCG 0.010% NA no6 0.358 GCCCGA 0.016% NA no 6 0.050 GCCCGC 0.010% NA no 6 −0.827 GCCCGG0.012%  0.337 no 6 −0.658 GCCTAA 0.021% −0.647 no 6 −1.440 GCCTAC 0.012%NA no 6 −0.634 GCCTAG 0.014% −0.583 no 6 −0.571 GCCTCA 0.017% NA no 6−1.086 GCCTCC 0.009% NA no 6 −0.243 GCCTCG 0.015%  0.277 no 6 −0.446GCCTGA 0.018% NA no 6 −0.038 GCCTGC 0.012%  0.260 no 6 −0.509 GCCTGG0.017%  0.174 no 6 −0.392 GCGAAA 0.045% NA no 6 −0.470 GCGAAC 0.028% 0.478 no 6 −0.177 GCGAAG 0.043%  0.358 no 6 0.338 GCGACA 0.028% NA no 6−0.690 GCGACC 0.016%  0.595 no 6 0.321 GCGACG 0.023%  0.718 no 6 0.170GCGAGA 0.034%  0.353 no 6 −0.578 GCGAGC 0.023%  0.331 no 6 −0.297 GCGAGG0.031% NA no 6 −0.506 GCGCAA 0.035% NA no 6 −0.479 GCGCAC 0.016%  0.375no 6 −0.288 GCGCAG 0.021% NA no 6 −0.199 GCGCCA 0.022%  0.434 no 6−0.253 GCGCCC 0.010%  0.289 no 6 −0.851 GCGCCG 0.010%  0.536 no 6 1.066GCGCGA 0.029%  0.506 no 6 −0.952 GCGCGC 0.010%  0.556 no 6 −0.880 GCGCGG0.017%  0.462 no 6 −0.572 GCGTAA 0.034% NA no 6 −0.710 GCGTAC 0.017% NAno 6 −0.423 GCGTAG 0.022% −0.428 no 6 0.175 GCGTCA 0.020% NA no 6 −0.702GCGTCC 0.012%  0.618 no 6 −1.056 GCGTCG 0.014%  0.676 no 6 0.218 GCGTGA0.024% NA no 6 0.073 GCGTGC 0.021%  0.128 no 6 0.219 GCGTGG 0.023% 0.287 no 6 0.105 GCTAAA 0.032% NA no 6 −1.867 GCTAAC 0.017% NA no 6−1.272 GCTAAG 0.027% −0.416 no 6 0.145 GCTACA 0.019% NA no 6 −0.911GCTACC 0.014% NA no 6 −0.258 GCTACG 0.023%  0.351 no 6 −0.409 GCTAGA0.024% NA no 6 −3.703 GCTAGC 0.014% −0.448 no 6 −4.537 GCTAGG 0.029%−0.764 no 6 −5.587 GCTCAA 0.027% NA no 6 −0.588 GCTCAC 0.018% NA no 60.296 GCTCAG 0.021% −0.343 no 6 −1.498 GCTCCA 0.021% NA no 6 −0.338GCTCCC 0.010% NA no 6 0.651 GCTCCG 0.010%  0.283 no 6 0.669 GCTCGA0.018% NA no 6 −1.157 GCTCGC 0.014% NA no 6 −0.417 GCTCGG 0.017%  0.150no 6 −0.412 GCTTAA 0.026% −0.508 no 6 −2.096 GCTTAC 0.014% NA no 6−1.977 GCTTAG 0.019% −0.606 no 6 −2.010 GCTTCA 0.014% NA no 6 −0.754GCTTCG 0.014%  0.412 no 6 −0.136 GCTTGA 0.019% NA no 6 −1.411 GCTTGC0.012% −0.236 no 6 −0.179 GCTTGG 0.012% NA no 6 1.196 GTCAAA 0.045% NAno 6 −0.412 GTCAAC 0.020% NA no 6 0.672 GTCAAG 0.032% NA no 6 −0.189GTCACA 0.030% NA no 6 −1.449 GTCACC 0.020% NA no 6 −0.815 GTCACG 0.024%NA no 6 −0.600 GTCAGA 0.039% NA no 6 −0.765 GTCAGC 0.020% −0.251 no 6−1.363 GTCAGG 0.044% −0.467 no 6 −1.558 GTCCAA 0.023% NA no 6 −1.184GTCCAC 0.015% NA no 6 −0.609 GTCCAG 0.023%  0.249 no 6 −0.943 GTCCCA0.014% −0.124 no 6 −1.573 GTCCCC 0.013% −0.215 no 6 −0.382 GTCCCG 0.011% 0.260 no 6 0.504 GTCCGA 0.014% NA no 6 −0.097 GTCCGC 0.010% NA no 61.157 GTCCGG 0.015%  0.422 no 6 0.354 GTCTAA 0.020% −0.418 no 6 0.162GTCTAC 0.013% NA no 6 −1.077 GTCTAG 0.019% −0.552 no 6 −0.533 GTCTCA0.016% NA no 6 −1.110 GTCTCC 0.012% NA no 6 −0.588 GTCTCG 0.019%  0.226no 6 0.787 GTCTGA 0.023% NA no 6 0.604 GTCTGC 0.018%  0.308 no 6 −4.146GTCTGG 0.024% NA no 6 0.134 GTGAAA 0.050%  0.237 yes 6 −3.116 GTGAAC0.035%  0.362 yes 6 −2.820 GTGAAG 0.047%  0.561 yes 6 −2.380 GTGACA0.037%  0.119 yes 6 −2.181 GTGACC 0.017%  0.335 yes 6 −1.395 GTGACG0.023%  0.584 yes 6 −3.743 GTGAGA 0.046%  0.363 yes 6 −3.601 GTGAGC0.031% NA yes 6 −3.323 GTGAGG 0.047% NA yes 6 −1.848 GTGCAA 0.034%−0.448 no 6 −1.188 GTGCAC 0.027% −0.066 no 6 −0.335 GTGCAG 0.024% −0.378no 6 −0.583 GTGCCA 0.019% −0.185 no 6 0.193 GTGCCC 0.013% −0.378 no 61.213 GTGCCG 0.013% NA no 6 −0.739 GTGCGA 0.023% NA no 6 0.420 GTGCGC0.013% NA no 6 −0.636 GTGCGG 0.030% NA no 6 0.075 GTGTAA 0.037% −0.335no 6 −1.019 GTGTAC 0.025% NA no 6 −0.619 GTGTAG 0.024% −0.504 no 6−0.551 GTGTCA 0.029% −0.246 no 6 −1.512 GTGTCC 0.013% NA no 6 0.463GTGTCG 0.020%  0.188 no 6 −0.356 GTGTGA 0.036%  0.125 no 6 −0.522 GTGTGC0.022% −0.174 no 6 0.097 GTGTGG 0.024% NA no 6 0.418 GTTAAA 0.041%−0.232 no 6 −3.467 GTTAAC 0.024% NA no 6 −3.293 GTTAAG 0.036% −0.390 no6 −0.661 GTTACA 0.032% NA no 6 −3.654 GTTACC 0.016%  0.258 no 6 −2.418GTTACG 0.017%  0.226 no 6 −0.631 GTTAGA 0.031% −0.551 no 6 −6.895 GTTAGC0.026% −0.483 no 6 −3.657 GTTAGG 0.028% −0.831 no 6 −9.046 GTTCAA 0.025% 0.224 no 6 −1.432 GTTCAC 0.015%  0.275 no 6 −0.576 GTTCAG 0.022% NA no6 −3.395 GTTCCA 0.019%  0.146 no 6 −0.906 GTTCCC 0.009% −0.385 no 6−1.074 GTTCCG 0.008%  0.212 no 6 1.510 GTTCGA 0.026%  0.508 no 6 −1.121GTTCGC 0.015%  0.589 no 6 −1.492 GTTCGG 0.016%  0.354 no 6 −0.379 GTTTAA0.035% −0.296 no 6 −3.228 GTTTAC 0.015% NA no 6 −2.741 GTTTAG 0.026%−0.622 no 6 −2.072 GTTTCA 0.019% NA no 6 −4.684 GTTTCC 0.008%  0.180 no6 −1.709 GTTTCG 0.015%  0.367 no 6 0.269 GTTTGA 0.025% NA no 6 −1.573GTTTGC 0.015% NA no 6 −1.237 GTTTGG 0.019% −0.200 no 6 0.065

TABLE 3 Effect sizes for the effects of each individual SNV in exon 18of BRCA1 on exon splicing/stability Library Library Library LibraryLibrary Library Average R1 R1 R R L L effect Repli- Repli- Repli- Repli-Repli- Repli- size (both cate 1 cate 2 cate 1 cate 2 cate 1 cate 2 Exonreps of MutPredSplice Mutation effect effect effect effect effect effectPosition Variant L and R) score MutPredSplice output Type size size sizesize size size 1 C −0.476 0.82 Splice Affecting Variant (SAV) sense NANA NA NA −0.577 −0.376 Loss of natural 3′ SS (P < 0.000001) 1 G −0.4930.9 Splice Affecting Variant (SAV) sense NA NA NA NA −0.839 −0.147 1 T−0.661 0.85 Splice Affecting Variant (SAV) sense NA NA NA NA −1.048−0.274 Loss of natural 3′ SS (P < 0.000001) 2 A −0.504 0.83 SpliceAffecting Variant (SAV) sense NA NA NA NA −0.529 −0.478 Loss of natural3′ SS (P < 0.000001) 2 C −0.630 0.85 Splice Affecting Variant (SAV)sense NA NA NA NA −0.746 −0.513 Loss of natural 3′ SS (P < 0.000001) 2 G−0.535 0.85 Splice Affecting Variant (SAV) sense NA NA NA NA −0.791−0.278 Loss of natural 3′ SS (P < 0.000001) 3 A −0.494 0.77 SpliceAffecting Variant (SAV) sense NA NA NA NA −0.528 −0.460 3 C −0.300 0.65Splice Affecting Variant (SAV) sense NA NA NA NA −0.022 −0.579 3 T−0.466 0.8 Splice Affecting Variant (SAV) sense NA NA NA NA −0.563−0.369 4 A −0.119 0.52 Splice Neutral Variant (SNV) sense NA NA NA NA−0.232 −0.007 4 G −0.432 0.95 Splice Affecting Variant (SAV) sense NA NANA NA −0.369 −0.495 Cryptic 5′ SS (P = 0.001003) 4 T −0.547 0.62 SpliceAffecting Variant (SAV) sense NA NA NA NA −0.300 −0.794 5 A −0.399 0.34Splice Neutral Variant (SNV) sense NA NA NA NA −0.599 −0.198 5 C −0.8410.39 Splice Neutral Variant (SNV) sense NA NA NA NA −0.824 −0.859 5 G−0.387 0.4 Splice Neutral Variant (SNV) sense NA NA NA NA −0.437 −0.3386 A −0.436 0.79 Splice Affecting Variant (SAV) sense NA NA NA NA −0.330−0.543 6 C −0.192 0.53 Splice Neutral Variant (SNV) sense NA NA NA NA−0.326 −0.058 6 T −2.084 0.88 Splice Affecting Variant (SAV) nonsense NANA NA NA −2.001 −2.167 ESS Gain (P < 0.000001) 7 C 0.044 0.39 SpliceNeutral Variant (SNV) sense NA NA NA NA 0.023 0.065 7 G −0.192 0.74Splice Affecting Variant (SAV) sense NA NA NA NA −0.293 −0.091 7 T−0.246 0.53 Splice Neutral Variant (SNV) sense NA NA NA NA −0.440 −0.0528 A −0.039 0.28 Splice Neutral Variant (SNV) sense NA NA NA NA 0.173−0.251 8 C −0.675 0.28 Splice Neutral Variant (SNV) sense NA NA NA NA−1.104 −0.246 8 T 0.092 0.35 Splice Neutral Variant (SNV) sense NA NA NANA 0.084 0.100 9 A −0.342 0.3 Splice Neutral Variant (SNV) sense NA NANA NA −0.551 −0.134 9 C −0.269 0.29 Splice Neutral Variant (SNV) senseNA NA NA NA −0.063 −0.475 9 G −0.294 0.48 Splice Neutral Variant (SNV)sense NA NA NA NA −0.288 −0.301 10 A −0.211 0.74 Splice AffectingVariant (SAV) sense NA NA NA NA −0.566 0.143 10 C −0.027 0.35 SpliceNeutral Variant (SNV) sense NA NA NA NA −0.457 0.403 10 G −0.138 0.39Splice Neutral Variant (SNV) sense NA NA NA NA −0.234 −0.043 11 A −0.7350.66 Splice Affecting Variant (SAV) sense NA NA NA NA −0.644 −0.827 11 C−0.391 0.35 Splice Neutral Variant (SNV) sense NA NA NA NA −0.277 −0.50411 G −0.171 0.72 Splice Affecting Variant (SAV) sense NA NA NA NA −0.169−0.172 12 A −0.191 0.56 Splice Neutral Variant (SNV) sense NA NA NA NA−0.355 −0.027 12 C −0.152 0.43 Splice Neutral Variant (SNV) sense NA NANA NA −0.301 −0.004 12 T −0.321 0.53 Splice Neutral Variant (SNV) senseNA NA NA NA −0.439 −0.203 13 A −0.088 0.44 Splice Neutral Variant (SNV)sense NA NA NA NA 0.001 −0.178 13 C −0.036 0.31 Splice Neutral Variant(SNV) sense NA NA NA NA −0.073 0.002 13 G −0.052 0.66 Splice AffectingVariant (SAV) sense NA NA NA NA −0.160 0.057 14 A −0.074 0.76 SpliceAffecting Variant (SAV) sense NA NA NA NA −0.009 −0.139 14 C −0.034 0.36Splice Neutral Variant (SNV) sense NA NA NA NA −0.153 0.085 14 T −0.0680.55 Splice Neutral Variant (SNV) sense NA NA NA NA −0.007 −0.130 15 A0.195 0.77 Splice Affecting Variant (SAV) sense NA NA NA NA 0.058 0.332Cryptic 5′ SS (P = 0.015766) 15 C −0.047 0.34 Splice Neutral Variant(SNV) sense NA NA NA NA −0.009 −0.084 15 G −0.111 0.56 Splice NeutralVariant (SNV) sense NA NA NA NA −0.185 −0.038 16 A 0.148 0.6 SpliceAffecting Variant (SAV) sense NA NA NA NA 0.103 0.192 16 C −0.020 0.33Splice Neutral Variant (SNV) sense NA NA NA NA −0.081 0.040 16 T −0.0470.59 Splice Neutral Variant (SNV) sense NA NA NA NA −0.123 0.028 17 A−1.387 0.4 Splice Neutral Variant (SNV) nonsense NA NA NA NA −1.483−1.292 17 C −0.058 0.35 Splice Neutral Variant (SNV) sense NA NA NA NA−0.038 −0.078 17 G −0.074 0.36 Splice Neutral Variant (SNV) sense NA NANA NA −0.085 −0.063 18 A −0.028 0.77 Splice Affecting Variant (SAV)sense NA NA NA NA 0.101 −0.156 18 C −0.194 0.36 Splice Neutral Variant(SNV) sense NA NA NA NA −0.368 −0.021 18 T −1.699 0.84 Splice AffectingVariant (SAV) nonsense NA NA NA NA −1.657 −1.740 ESE Loss (P = 0.046524)ESS Gain (P = 0.000732) 19 C −0.018 0.4 Splice Neutral Variant (SNV)sense NA NA NA NA −0.034 −0.003 19 G −0.069 0.39 Splice Neutral Variant(SNV) sense NA NA NA NA −0.117 −0.021 19 T 0.226 0.77 Splice AffectingVariant (SAV) sense NA NA NA NA 0.238 0.214 ESE Loss (P = 0.004064) 20 C0.054 0.33 Splice Neutral Variant (SNV) sense NA NA NA NA 0.047 0.060 20G 0.049 0.49 Splice Neutral Variant (SNV) sense NA NA NA NA −0.096 0.19320 T 0.131 0.49 Splice Neutral Variant (SNV) sense NA NA NA NA 0.0590.204 21 A 0.194 0.42 Splice Neutral Variant (SNV) sense NA NA NA NA0.000 0.389 21 G 0.005 0.58 Splice Neutral Variant (SNV) sense NA NA NANA 0.005 0.005 21 T −0.529 0.53 Splice Neutral Variant (SNV) sense NA NANA NA −1.231 0.174 22 A 0.169 0.41 Splice Neutral Variant (SNV) sense NANA NA NA 0.225 0.114 22 C 0.064 0.33 Splice Neutral Variant (SNV) senseNA NA NA NA 0.113 0.015 22 T −0.232 0.37 Splice Neutral Variant (SNV)sense NA NA NA NA −0.272 −0.193 23 A 0.134 0.39 Splice Neutral Variant(SNV) sense NA NA NA NA 0.047 0.221 23 C 0.270 0.58 Splice NeutralVariant (SNV) sense NA NA NA NA 0.419 0.121 23 T 0.164 0.58 SpliceNeutral Variant (SNV) sense NA NA NA NA 0.254 0.075 24 C 0.187 0.59Splice Neutral Variant (SNV) sense NA NA NA NA 0.040 0.335 24 G 0.1610.54 Splice Neutral Variant (SNV) sense NA NA NA NA 0.132 0.190 24 T0.071 0.67 Splice Affecting Variant (SAV) sense NA NA NA NA 0.062 0.081ESE Loss (P = 0.000173) 25 A 0.098 0.35 Splice Neutral Variant (SNV)sense NA NA NA NA 0.241 −0.044 25 G 0.046 0.35 Splice Neutral Variant(SNV) sense NA NA NA NA −0.041 0.133 25 T −0.084 0.57 Splice NeutralVariant (SNV) sense NA NA NA NA −0.145 −0.023 26 C 0.031 0.29 SpliceNeutral Variant (SNV) sense NA NA NA NA 0.167 −0.105 26 G −0.155 0.39Splice Neutral Variant (SNV) sense NA NA NA NA −0.177 −0.134 26 T −0.0880.34 Splice Neutral Variant (SNV) sense NA NA NA NA −0.041 −0.134 27 A−0.154 0.44 Splice Neutral Variant (SNV) sense NA NA NA NA −0.216 −0.09127 G 0.235 0.5 Splice Neutral Variant (SNV) sense NA NA NA NA 0.1320.337 27 T −0.144 0.36 Splice Neutral Variant (SNV) sense NA NA NA NA−0.173 −0.116 28 A −0.071 0.36 Splice Neutral Variant (SNV) sense NA NANA NA −0.017 −0.125 28 C −0.334 0.34 Splice Neutral Variant (SNV) senseNA NA NA NA −0.646 −0.022 28 G −0.181 0.37 Splice Neutral Variant (SNV)sense NA NA NA NA −0.363 0.002 29 A 0.000 0.76 Splice Affecting Variant(SAV) sense NA NA NA NA 0.082 −0.081 ESE Loss (P = 0.046524) ESS Gain (P= 0.034846) 29 C 0.010 0.48 Splice Neutral Variant (SNV) sense NA NA NANA 0.073 −0.053 29 T −0.537 0.8 Splice Affecting Variant (SAV) sense NANA NA NA −0.637 −0.436 ESE Loss (P = 0.046524) ESS Gain (P = 0.034846)30 C −0.039 0.43 Splice Neutral Variant (SNV) sense NA NA NA NA −0.2790.201 30 G 0.109 0.31 Splice Neutral Variant (SNV) sense NA NA NA NA0.284 −0.065 30 T −1.353 0.82 Splice Affecting Variant (SAV) nonsense NANA NA NA −1.626 −1.081 Cryptic 3′ SS (P = 0.03882) 31 C −0.205 0.37Splice Neutral Variant (SNV) sense NA NA NA NA −0.211 −0.199 31 G 0.0290.33 Splice Neutral Variant (SNV) sense NA NA NA NA −0.102 0.160 31 T−0.006 0.49 Splice Neutral Variant (SNV) sense NA NA NA NA −0.074 0.06232 C 0.228 0.28 Splice Neutral Variant (SNV) sense NA NA NA NA 0.3670.088 32 G −0.067 0.45 Splice Neutral Variant (SNV) sense NA NA NA NA−0.015 −0.118 32 T −0.097 0.38 Splice Neutral Variant (SNV) sense NA NANA NA −0.006 −0.188 33 A 0.189 0.28 Splice Neutral Variant (SNV) senseNA NA NA NA 0.023 0.355 33 C −0.057 0.26 Splice Neutral Variant (SNV)sense NA NA NA NA 0.055 −0.169 33 G −0.078 0.28 Splice Neutral Variant(SNV) sense NA NA NA NA −0.683 0.527 34 C 0.085 0.31 Splice NeutralVariant (SNV) sense NA NA NA NA 0.066 0.104 34 G 0.207 0.45 SpliceNeutral Variant (SNV) sense NA NA NA NA 0.163 0.252 34 T −0.180 0.37Splice Neutral Variant (SNV) sense NA NA NA NA −0.300 −0.061 35 A −1.1300.36 Splice Neutral Variant (SNV) nonsense NA NA NA NA −0.842 −1.417 35C 0.041 0.29 Splice Neutral Variant (SNV) sense NA NA NA NA 0.087 −0.00435 G −1.279 0.51 Splice Neutral Variant (SNV) nonsense NA NA NA NA−1.364 −1.195 36 A −0.023 0.36 Splice Neutral Variant (SNV) sense NA NANA NA −0.065 0.018 36 C 0.039 0.32 Splice Neutral Variant (SNV) sense NANA NA NA 0.243 −0.165 36 G 0.024 0.37 Splice Neutral Variant (SNV) senseNA NA NA NA −0.028 0.077 37 A 0.111 0.37 Splice Neutral Variant (SNV)sense NA NA NA NA 0.170 0.052 37 C −0.137 0.33 Splice Neutral Variant(SNV) sense NA NA NA NA −0.455 0.180 37 G −0.309 0.33 Splice NeutralVariant (SNV) sense NA NA NA NA −0.270 −0.347 38 A −0.010 0.42 SpliceNeutral Variant (SNV) sense NA NA NA NA −0.295 0.276 38 C 0.100 0.34Splice Neutral Variant (SNV) sense NA NA NA NA 0.050 0.149 38 G −0.1460.36 Splice Neutral Variant (SNV) sense NA NA NA NA −0.382 0.090 39 A−0.034 0.44 Splice Neutral Variant (SNV) sense NA NA NA NA −0.106 0.03839 G −0.073 0.47 Splice Neutral Variant (SNV) sense NA NA NA NA −0.053−0.093 39 T −0.130 0.49 Splice Neutral Variant (SNV) sense NA NA NA NA0.055 −0.315 40 A 0.273 0.31 Splice Neutral Variant (SNV) sense 0.857−0.291 0.164 1.299 −0.084 −0.285 40 C 0.157 0.35 Splice Neutral Variant(SNV) sense 1.050 0.107 0.496 0.146 −0.075 0.063 40 G 0.031 0.32 SpliceNeutral Variant (SNV) sense 1.239 0.694 −0.122 0.185 −0.102 0.164 41 C−0.008 0.32 Splice Neutral Variant (SNV) sense 0.475 0.340 0.578 −0.178−0.212 −0.219 41 G 0.057 0.4 Splice Neutral Variant (SNV) sense 0.0420.078 0.515 0.253 −0.030 −0.509 41 T 0.094 0.32 Splice Neutral Variant(SNV) nonsense −0.027 0.287 0.170 0.267 −0.101 0.042 42 A −0.166 0.42Splice Neutral Variant (SNV) sense −0.084 0.671 −0.288 0.034 −0.4130.004 42 C 0.102 0.36 Splice Neutral Variant (SNV) sense 0.308 0.0900.109 0.139 −0.154 0.312 42 T −1.417 0.48 Splice Neutral Variant (SNV)sense −1.140 −0.760 −1.491 −1.723 −1.501 −0.952 43 A 0.117 0.34 SpliceNeutral Variant (SNV) sense 0.145 0.495 −0.119 0.195 0.065 0.326 43 C0.151 0.42 Splice Neutral Variant (SNV) sense 0.046 0.608 0.110 0.431−0.057 0.119 43 T −0.377 0.8 Splice Affecting Variant (SAV) sense −0.071−0.219 −1.125 −0.950 0.162 0.404 44 C −0.047 0.48 Splice Neutral Variant(SNV) sense 0.044 0.120 −0.235 0.157 0.293 −0.402 44 G −0.824 0.53Splice Neutral Variant (SNV) sense 0.041 0.049 −1.455 −0.786 −0.884−0.171 44 T −0.616 0.96 Splice Affecting Variant (SAV) sense −0.1620.335 −1.208 −0.547 −0.569 −0.141 ESS Gain (P = 0.000003) Cryptic 5′ SS(P = 0.018361) 45 C 0.114 0.37 Splice Neutral Variant (SNV) sense 0.0790.109 0.087 0.141 NA NA 45 G −0.257 0.42 Splice Neutral Variant (SNV)sense 0.178 0.241 −0.316 −0.198 NA NA 45 T 0.120 0.46 Splice NeutralVariant (SNV) sense 0.046 −0.011 0.029 0.211 NA NA 46 A 0.055 0.43Splice Neutral Variant (SNV) sense 0.352 0.488 −0.328 0.437 NA NA 46 C0.966 0.24 Splice Neutral Variant (SNV) sense 0.244 0.316 0.550 1.382 NANA 46 G 0.071 0.36 Splice Neutral Variant (SNV) sense 0.207 0.183 −0.0300.173 NA NA 47 A 0.149 0.46 Splice Neutral Variant (SNV) sense 0.064−0.220 0.395 −0.097 NA NA 47 C 0.234 0.26 Splice Neutral Variant (SNV)sense 0.252 0.660 −0.031 0.499 NA NA 47 G −0.494 0.35 Splice NeutralVariant (SNV) sense −0.272 0.232 −0.588 −0.400 NA NA 48 A 0.211 0.42Splice Neutral Variant (SNV) sense −0.183 0.321 0.127 0.294 NA NA 48 C0.222 0.3 Splice Neutral Variant (SNV) sense 0.099 0.208 0.031 0.414 NANA 48 T 0.138 0.37 Splice Neutral Variant (SNV) sense 0.072 0.146 0.1530.124 NA NA 49 A −0.759 0.36 Splice Neutral Variant (SNV) sense −0.3320.288 −0.610 −0.909 NA NA 49 G −2.574 0.61 Splice Affecting Variant(SAV) sense −1.447 −1.282 −2.905 −2.243 NA NA 49 T −0.784 0.48 SpliceNeutral Variant (SNV) sense −0.264 −0.202 −0.877 −0.692 NA NA 50 A 0.4500.36 Splice Neutral Variant (SNV) sense 0.532 0.158 0.310 0.590 NA NA 50C 0.106 0.25 Splice Neutral Variant (SNV) sense 0.158 0.629 0.075 0.137NA NA 50 T 0.255 0.25 Splice Neutral Variant (SNV) sense 0.152 0.1980.382 0.127 NA NA 51 A 0.408 0.29 Splice Neutral Variant (SNV) sense0.194 −0.245 0.265 0.551 NA NA 51 C 0.567 0.33 Splice Neutral Variant(SNV) sense 0.337 −0.034 0.767 0.367 NA NA 51 T −1.076 0.54 SpliceNeutral Variant (SNV) nonsense −1.157 −0.704 −0.905 −1.248 NA NA 52 A0.039 0.34 Splice Neutral Variant (SNV) sense −0.027 0.076 0.100 −0.022NA NA 52 C 0.476 0.43 Splice Neutral Variant (SNV) sense 0.079 −0.0610.484 0.468 NA NA 52 T −0.334 0.92 Splice Affecting Variant (SAV) sense−0.340 −0.502 −0.268 −0.400 NA NA Cryptic 5′ SS (P = 0.009018) 53 C−0.048 0.4 Splice Neutral Variant (SNV) sense 0.298 0.836 −0.067 −0.028NA NA 53 G −1.757 0.69 Splice Affecting Variant (SAV) sense −0.949−0.312 −1.933 −1.580 NA NA ESE Loss (P = 0.046524) ESS Gain (P =0.034846) 53 T −0.070 0.46 Splice Neutral Variant (SNV) sense 0.3030.246 −0.077 −0.062 NA NA 54 A 0.470 0.43 Splice Neutral Variant (SNV)sense −0.303 −0.264 0.035 0.905 NA NA 54 C 0.222 0.4 Splice NeutralVariant (SNV) sense 0.186 0.551 0.448 −0.004 NA NA 54 T −0.673 0.47Splice Neutral Variant (SNV) nonsense −1.089 −0.743 −0.796 −0.549 NA NA55 A 0.796 0.5 Splice Neutral Variant (SNV) sense 0.193 0.075 0.5081.083 NA NA 55 C 0.140 0.43 Splice Neutral Variant (SNV) sense 0.171−0.046 −0.201 0.481 NA NA 55 T 0.073 0.84 Splice Affecting Variant (SAV)sense 0.062 0.357 0.219 −0.073 NA NA ESE Loss (P = 0.004064) ESS Gain (P= 0.034846) 56 C −0.464 0.57 Splice Neutral Variant (SNV) sense 0.3800.579 −0.466 −0.463 NA NA 56 G −1.586 0.75 Splice Affecting Variant(SAV) sense −1.392 −0.978 −1.516 −1.656 NA NA ESE Loss (P = 0.004064) 56T −0.926 0.98 Splice Affecting Variant (SAV) sense −0.836 −1.042 −0.923−0.930 NA NA ESE Loss (P = 0.004064) Cryptic 5′ SS (P = 0.003403) 57 C0.275 0.31 Splice Neutral Variant (SNV) sense 0.617 0.091 0.063 0.488 NANA 57 G −0.159 0.31 Splice Neutral Variant (SNV) sense 0.028 0.147−0.594 0.276 NA NA 57 T −1.998 0.62 Splice Affecting Variant (SAV)nonsense −1.675 −1.613 −1.949 −2.048 NA NA 58 C −0.181 0.29 SpliceNeutral Variant (SNV) sense 0.206 −0.031 −0.209 −0.154 NA NA 58 G −0.0680.35 Splice Neutral Variant (SNV) sense 0.657 0.338 0.009 −0.145 NA NA58 T 0.344 0.44 Splice Neutral Variant (SNV) sense 0.149 0.321 0.2460.441 NA NA 59 C −0.037 0.31 Splice Neutral Variant (SNV) sense −0.1100.042 0.427 −0.500 NA NA 59 G −0.192 0.56 Splice Neutral Variant (SNV)sense −0.067 −0.130 −0.366 −0.017 NA NA 59 T 0.137 0.41 Splice NeutralVariant (SNV) sense −0.332 −0.015 0.283 −0.010 NA NA 60 A 0.046 0.58Splice Neutral Variant (SNV) sense 0.350 0.033 −0.102 0.193 NA NA 60 C0.325 0.58 Splice Neutral Variant (SNV) sense 0.079 −0.308 0.517 0.133NA NA 60 G −0.473 0.59 Splice Neutral Variant (SNV) sense −0.622 −0.343−0.440 −0.505 NA NA 61 A −2.485 0.84 Splice Affecting Variant (SAV)nonsense −1.871 −1.798 −2.150 −2.820 NA NA 61 C 0.504 0.6 SpliceAffecting Variant (SAV) sense −0.015 0.149 0.396 0.612 NA NA ESS Loss (P< 0.000001) 61 T 0.316 0.56 Splice Neutral Variant (SNV) sense 0.2780.295 0.448 0.184 NA NA 62 A −0.827 0.61 Splice Affecting Variant (SAV)nonsense −0.638 −0.412 −0.674 −0.980 NA NA ESS Loss (P < 0.000001) 62 C0.112 0.52 Splice Neutral Variant (SNV) sense 0.367 0.571 0.120 0.105 NANA 62 T 0.737 0.55 Splice Neutral Variant (SNV) sense 0.396 −0.456 0.8240.651 NA NA 63 A 0.133 0.39 Splice Neutral Variant (SNV) sense 0.5700.316 0.311 −0.045 NA NA 63 C −0.144 0.44 Splice Neutral Variant (SNV)sense 0.897 0.597 0.087 −0.374 NA NA 63 T −2.229 0.82 Splice AffectingVariant (SAV) sense −2.707 −2.655 −2.037 −2.421 NA NA Cryptic 5′ SS (P =0.007933) 64 A 0.247 0.53 Splice Neutral Variant (SNV) sense 0.153−0.203 0.031 0.463 NA NA 64 C 0.260 0.47 Splice Neutral Variant (SNV)sense 0.505 1.164 −0.026 0.546 NA NA 64 G −0.056 0.55 Splice NeutralVariant (SNV) sense −0.095 0.672 −0.656 0.544 NA NA 65 C 0.535 0.44Splice Neutral Variant (SNV) sense 0.917 0.447 0.258 0.813 NA NA 65 G0.291 0.54 Splice Neutral Variant (SNV) sense 0.271 0.442 0.517 0.064 NANA 65 T 0.362 0.5 Splice Neutral Variant (SNV) sense 0.152 0.415 0.3770.348 NA NA 66 A −0.386 0.87 Splice Affecting Variant (SAV) sense −0.490−0.570 −0.088 −0.684 NA NA Cryptic 5′ SS (P = 0.013422) 66 C 0.301 0.7Splice Affecting Variant (SAV) sense 0.393 0.115 0.104 0.499 NA NA 66 T0.217 0.75 Splice Affecting Variant (SAV) sense 0.202 0.131 0.149 0.285NA NA 67 A −0.154 0.59 Splice Neutral Variant (SNV) sense 0.125 0.081−0.431 0.123 NA NA 67 C 0.117 0.55 Splice Neutral Variant (SNV) sense0.012 0.052 0.138 0.096 NA NA 67 G −4.136 0.93 Splice Affecting Variant(SAV) sense −4.512 −3.529 −3.967 −4.306 NA NA Cryptic 5′ SS (P =0.009018) 68 A −0.097 0.75 Splice Affecting Variant (SAV) sense 0.0110.173 0.289 −0.483 NA NA 68 C 0.054 0.37 Splice Neutral Variant (SNV)sense 0.367 0.025 0.248 −0.140 NA NA 68 G 0.102 0.48 Splice NeutralVariant (SNV) sense 0.211 0.111 0.297 −0.093 NA NA 69 C 0.001 0.4 SpliceNeutral Variant (SNV) sense 0.300 −0.419 0.124 −0.122 NA NA 69 G −0.1310.38 Splice Neutral Variant (SNV) sense 0.061 0.140 −0.251 −0.011 NA NA69 T −0.030 0.57 Splice Neutral Variant (SNV) sense −0.008 −0.170 −0.1370.076 NA NA 70 A −0.212 0.58 Splice Neutral Variant (SNV) sense 0.019−0.386 −0.182 −0.242 NA NA 70 C −0.191 0.38 Splice Neutral Variant (SNV)sense −0.334 −0.909 −0.001 −0.381 NA NA 70 T −0.159 0.56 Splice NeutralVariant (SNV) sense −0.217 0.183 0.087 −0.405 NA NA 71 A −0.020 0.59Splice Neutral Variant (SNV) sense 0.433 0.021 −0.712 0.671 NA NA 71 G−0.547 0.97 Splice Affecting Variant (SAV) sense −0.203 −0.771 −0.761−0.332 NA NA ESS Gain (P < 0.000001) Cryptic 5′ SS (P = 0.021088) 71 T−0.325 0.76 Splice Affecting Variant (SAV) sense 0.060 0.257 −0.317−0.332 NA NA ESS Gain (P < 0.000001) 72 A −0.320 0.32 Splice NeutralVariant (SNV) sense 0.623 0.348 −0.168 −0.473 NA NA 72 C 0.106 0.34Splice Neutral Variant (SNV) sense −0.167 0.024 −0.017 0.229 NA NA 72 G−0.044 0.37 Splice Neutral Variant (SNV) sense 0.627 0.199 −0.086 −0.002NA NA 73 C 0.234 0.35 Splice Neutral Variant (SNV) sense 0.181 0.1190.491 −0.024 NA NA 73 G 0.089 0.34 Splice Neutral Variant (SNV) sense0.352 0.113 −0.248 0.427 NA NA 73 T −0.229 0.4 Splice Neutral Variant(SNV) sense 0.103 0.196 0.013 −0.471 NA NA 74 A −1.758 0.45 SpliceNeutral Variant (SNV) nonsense −0.942 −1.421 −1.427 −2.090 NA NA 74 C−0.153 0.37 Splice Neutral Variant (SNV) sense −0.153 −0.065 −0.100−0.206 NA NA 74 G −2.168 0.59 Splice Neutral Variant (SNV) nonsense−1.380 −1.661 −2.321 −2.016 NA NA 75 A 0.422 0.51 Splice Neutral Variant(SNV) sense 0.847 0.405 0.340 0.504 NA NA 75 C 0.019 0.45 Splice NeutralVariant (SNV) sense 0.624 0.503 −0.035 0.073 NA NA 75 G 0.415 0.54Splice Neutral Variant (SNV) sense 0.206 0.384 0.577 0.253 NA NA 76 A−0.002 0.69 Splice Affecting Variant (SAV) sense −0.103 0.311 −0.3280.323 NA NA 76 C 0.100 0.75 Splice Affecting Variant (SAV) sense −0.023−0.306 −0.132 0.332 NA NA 76 G −0.031 0.68 Splice Affecting Variant(SAV) sense 0.441 0.298 −0.362 0.301 NA NA 77 A −0.095 0.85 SpliceAffecting Variant (SAV) sense −0.386 −0.936 0.220 −0.409 NA NA Loss ofnatural 5′ SS (P < 0.000001) 77 G −0.005 0.85 Splice Affecting Variant(SAV) sense 0.318 0.769 −0.223 0.213 NA NA 77 T −0.564 0.85 SpliceAffecting Variant (SAV) sense 0.094 −0.340 −0.385 −0.743 NA NA 78 A−0.277 0.82 Splice Affecting Variant (SAV) sense −0.094 −0.418 0.054−0.608 NA NA 78 C −0.024 0.82 Splice Affecting Variant (SAV) sense−0.269 0.327 0.170 −0.219 NA NA 78 G 0.686 0.83 Splice Affecting Variant(SAV) sense −0.004 0.512 0.753 0.620 NA NA

TABLE 4Emprical measurement of the effects of genome edits to exon 2 of DBR1 on cellular growth

Gray rows indicate missing data across both replicates

What is claimed is:
 1. A method for introducing a plurality ofprogrammed nucleotide modifications into a single locus of a desiredgenomic DNA sequence, comprising: (a) synthesizing a homology-directedrepair (HDR) library comprising a plurality of oligonucleotides, whereineach oligonucleotide comprises a programmed nucleotide modification inthe locus of the desired genome; and (b) co-transfecting a population ofcells with (i) an expression system capable of expressing Cas9 and asingle guide RNA (sgRNA), and (ii) the HDR library, wherein theexpression system is capable of introducing the plurality ofoligonucleotides having the programmed nucleotide modifications to thelocus of the desired genomic DNA sequence in one or more cells of thepopulation; wherein the method is carried out in a single experiment. 2.The method of claim 1, wherein each programmed nucleotide modificationis a single nucleotide variant.
 3. The method of claim 1, wherein theHDR library is constructed using an oligonucleotide comprising adegenerate sequence.
 4. The method of claim 3, wherein the degeneratesequence is between 1 and 100 nucleotides in length.
 5. The method ofclaim 4, wherein the HDR library comprises a set of oligonucleotideshaving at least 100 unique programmed nucleotide modifications, a least200 unique programmed nucleotide modifications, at least 300 uniqueprogrammed nucleotide modifications, at least 400 unique programmednucleotide modifications, at least 500 unique programmed nucleotidemodifications, at least 600 unique programmed nucleotide modifications,at least 700 unique programmed nucleotide modifications, at least 800unique programmed nucleotide modifications, at least 900 uniqueprogrammed nucleotide modifications, at least 1,000 unique programmednucleotide modifications, at least 3,000 unique programmed nucleotidemodifications, at least 4,000 unique programmed nucleotidemodifications, at least 5,000 unique programmed nucleotidemodifications, at least 6,000 unique programmed nucleotidemodifications, at least 7,000 unique programmed nucleotidemodifications, at least 8,000 unique programmed nucleotidemodifications, at least 9,000 unique programmed nucleotidemodifications, at least 10,000 unique programmed nucleotidemodifications, at least 12,000 unique programmed nucleotidemodifications, at least 14,000 unique programmed nucleotidemodifications, at least 16,000 unique programmed nucleotidemodifications, at least 18,000 unique programmed nucleotidemodifications, at least 20,000 unique programmed nucleotidemodifications, at least 25,000 unique programmed nucleotidemodifications, at least 30,000 unique programmed nucleotidemodifications, at least 40,000 unique programmed nucleotidemodifications, or at least 50,000 unique programmed nucleotidemodifications.
 6. The method of claim 1, wherein the plurality ofprogrammed nucleotide modifications that are introduced to the locus ofthe desired genomic DNA sequence results in a saturating set ofprogrammed nucleotide modifications.
 7. The method of claim 1, whereinthe plurality of oligonucleotides are synthesized on a microarray or incolumn-based synthesis.
 8. The method of claim 1, wherein the expressionsystem comprises a plasmid which comprises (i) a Cas9 expressioncassette that includes a nucleotide sequence which encodes a Cas9nuclease, (ii) an sgRNA expression cassette, and (iii) aspecies-specific promoter that is specific to the population of cells.9. The method of claim 1, further comprising cloning the HDR libraryprior to the step of co-transfecting the population of cells.
 10. Themethod of claim 1, wherein each oligonucleotide of the HDR libraryfurther comprises a pair of homology arms.
 11. The method of claim 1,further comprising (c) harvesting the population of cells, (d)selectively amplifying a genomic DNA and RNA sample, wherein the editedsequences are amplified and the non-edited sequence are not amplified,and (e) sequencing the genomic DNA and RNA sample that has beenselectively amplified, resulting in a set of genomic transcripts whichinclude the plurality of programmed nucleotide modifications.
 12. Themethod of claim 11, further comprising functionally analyzing the set ofgenomic transcripts using a functional assay.
 13. The method of claim12, wherein the functional assay is selected from the group consistingof targeted RNA sequencing to measure transcript abundance, targeted DNAsequencing to measure reduced cellular fitness, targeted chromatinimmunoprecipitation-sequencing (CHiP-seq) of co-activators to assayenhancers, increased cellular growth rate to assay cancer drivers ordrug resistance, and FACS-based phenotypic sorting for cellular assays.14. A method for analyzing the functional consequence of a genomicmutation comprising: (a) synthesizing a homology-directed repair (HDR)library comprising a plurality of oligonucleotides, wherein eacholigonucleotide comprises a programmed nucleotide modification in thelocus of the desired genome; (b) co-transfecting a population of cellswith (i) an expression system capable of expressing Cas9 and a guide RNA(sgRNA) and (ii) the HDR library, wherein the expression system iscapable of introducing the plurality of oligonucleotides having theprogrammed nucleotide modifications to the locus of the desired genomicDNA sequence in one or more cells of the population; (c) harvesting thepopulation of cells; (d) selectively amplifying a genomic DNA and RNAsample, wherein the edited sequences are amplified and the non-editedsequence are not amplified; (e) sequencing the genomic DNA and RNAsample that has been selectively amplified, resulting in a set ofgenomic transcripts which include the plurality of programmed nucleotidemodifications; and (f) functionally analyzing the set of genomictranscripts using a functional assay; wherein the method is carried outin a single experiment.
 15. The method of claim 14, wherein the HDRlibrary is constructed using an oligonucleotide comprising a degeneratesequence, wherein the degenerate sequence is between 1 and 100nucleotides in length.
 16. The method of claim 14, wherein the pluralityof oligonucleotides are synthesized on a microarray or in column-basedsynthesis.
 17. The method of claim 14, wherein the expression systemcomprises a plasmid which comprises (i) a Cas9 expression cassette thatincludes a nucleotide sequence which encodes a Cas9 nuclease, (ii) ansgRNA expression cassette, and (iii) a species-specific promoter that isspecific to the population of cells.
 18. The method of claim 14, whereinthe functional assay is selected from the group consisting of targetedRNA sequencing to measure transcript abundance, targeted DNA sequencingto measure reduced cellular fitness, targeted chromatinimmunoprecipitation-sequencing (CHiP-seq) of co-activators to assayenhancers, increased cellular growth rate to assay cancer drivers ordrug resistance, and FACS-based phenotypic sorting for cellular assays.19. A method for genomic screening, comprising: (a) introducing aplurality of programmed nucleotide modifications to a single genomiclocus in a single experiment, wherein step (a) comprises the method ofclaim 1; (b) sequencing the genomic DNA or cDNA of the edited locus; and(c) quantifying the transcript abundance of each mutation.
 20. Themethod of claim 19, wherein step (c) comprises calculating an enrichmentscore for each mutation.